TW205034B - - Google Patents
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- TW205034B TW205034B TW080107221A TW80107221A TW205034B TW 205034 B TW205034 B TW 205034B TW 080107221 A TW080107221 A TW 080107221A TW 80107221 A TW80107221 A TW 80107221A TW 205034 B TW205034 B TW 205034B
- Authority
- TW
- Taiwan
- Prior art keywords
- compound
- bis
- butyl
- fluorophenyl
- trap
- Prior art date
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- 125000000217 alkyl group Chemical group 0.000 claims abstract description 18
- 150000003839 salts Chemical class 0.000 claims abstract description 16
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 12
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 8
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 6
- 239000004480 active ingredient Substances 0.000 claims abstract description 5
- 125000001624 naphthyl group Chemical group 0.000 claims abstract description 3
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 6
- 125000005843 halogen group Chemical group 0.000 claims description 6
- 239000004305 biphenyl Substances 0.000 claims description 4
- 206010020772 Hypertension Diseases 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 3
- 239000005557 antagonist Substances 0.000 claims description 3
- 235000010290 biphenyl Nutrition 0.000 claims description 3
- 125000006267 biphenyl group Chemical group 0.000 claims description 3
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 3
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 claims description 2
- 230000017531 blood circulation Effects 0.000 claims description 2
- 229910001424 calcium ion Inorganic materials 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 125000004434 sulfur atom Chemical group 0.000 claims description 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 3
- 208000031481 Pathologic Constriction Diseases 0.000 claims 1
- 235000004522 Pentaglottis sempervirens Nutrition 0.000 claims 1
- 125000003172 aldehyde group Chemical group 0.000 claims 1
- 230000002490 cerebral effect Effects 0.000 claims 1
- 230000004087 circulation Effects 0.000 claims 1
- 239000000049 pigment Substances 0.000 claims 1
- 208000037804 stenosis Diseases 0.000 claims 1
- 230000036262 stenosis Effects 0.000 claims 1
- 238000003971 tillage Methods 0.000 claims 1
- -1 nitro, amino, hydroxy Chemical group 0.000 abstract description 106
- 239000003814 drug Substances 0.000 abstract description 13
- 229940079593 drug Drugs 0.000 abstract description 10
- 125000003710 aryl alkyl group Chemical group 0.000 abstract description 7
- 125000003118 aryl group Chemical group 0.000 abstract description 7
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract description 7
- 125000002252 acyl group Chemical group 0.000 abstract description 4
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 abstract description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract description 4
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract description 4
- 229910052736 halogen Inorganic materials 0.000 abstract description 3
- 150000002367 halogens Chemical class 0.000 abstract description 3
- 125000001424 substituent group Chemical group 0.000 abstract description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract description 3
- 125000002102 aryl alkyloxo group Chemical group 0.000 abstract description 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract description 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- LLZRSOPHIGKISM-UHFFFAOYSA-N 1,4-diphenylpiperazine Chemical class C1CN(C=2C=CC=CC=2)CCN1C1=CC=CC=C1 LLZRSOPHIGKISM-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 210000000056 organ Anatomy 0.000 abstract 1
- 239000011593 sulfur Substances 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 105
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 description 96
- 241000009298 Trigla lyra Species 0.000 description 88
- 150000001875 compounds Chemical class 0.000 description 84
- 238000005481 NMR spectroscopy Methods 0.000 description 63
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 60
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 57
- 238000011049 filling Methods 0.000 description 48
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 47
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 45
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 39
- 239000000126 substance Substances 0.000 description 33
- 238000002844 melting Methods 0.000 description 31
- 230000008018 melting Effects 0.000 description 31
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 28
- 239000007937 lozenge Substances 0.000 description 28
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 24
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 21
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 21
- BTVVEKSXUOEVAY-UHFFFAOYSA-N 4,4-diphenylpiperidine Chemical class C1CNCCC1(C=1C=CC=CC=1)C1=CC=CC=C1 BTVVEKSXUOEVAY-UHFFFAOYSA-N 0.000 description 20
- 239000007789 gas Substances 0.000 description 20
- 239000002904 solvent Substances 0.000 description 20
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 18
- 239000011575 calcium Substances 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- 239000012046 mixed solvent Substances 0.000 description 17
- 239000003826 tablet Substances 0.000 description 17
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 16
- 229910052791 calcium Inorganic materials 0.000 description 16
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 16
- 239000000243 solution Substances 0.000 description 16
- 239000007788 liquid Substances 0.000 description 15
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 12
- 238000003756 stirring Methods 0.000 description 12
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 11
- 230000002079 cooperative effect Effects 0.000 description 11
- 239000003054 catalyst Substances 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 10
- 239000013078 crystal Substances 0.000 description 10
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- 239000002253 acid Substances 0.000 description 9
- 239000002585 base Substances 0.000 description 9
- 238000003818 flash chromatography Methods 0.000 description 9
- 239000003921 oil Substances 0.000 description 9
- 235000019198 oils Nutrition 0.000 description 9
- 230000008485 antagonism Effects 0.000 description 8
- 238000001035 drying Methods 0.000 description 8
- 238000002329 infrared spectrum Methods 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 238000004809 thin layer chromatography Methods 0.000 description 8
- 238000012360 testing method Methods 0.000 description 7
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 6
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 6
- 229940125898 compound 5 Drugs 0.000 description 6
- 238000001819 mass spectrum Methods 0.000 description 6
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 6
- 238000011282 treatment Methods 0.000 description 6
- 229920002261 Corn starch Polymers 0.000 description 5
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 206010041349 Somnolence Diseases 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 229940125782 compound 2 Drugs 0.000 description 5
- 239000008120 corn starch Substances 0.000 description 5
- 125000005982 diphenylmethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 5
- 239000012153 distilled water Substances 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 239000007924 injection Substances 0.000 description 5
- 238000002347 injection Methods 0.000 description 5
- 239000008101 lactose Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 5
- 239000000741 silica gel Substances 0.000 description 5
- 229910002027 silica gel Inorganic materials 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 4
- 241000700159 Rattus Species 0.000 description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 4
- 238000004440 column chromatography Methods 0.000 description 4
- 229940126214 compound 3 Drugs 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- QUSNBJAOOMFDIB-UHFFFAOYSA-N monoethyl amine Natural products CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 4
- DEVSOMFAQLZNKR-RJRFIUFISA-N (z)-3-[3-[3,5-bis(trifluoromethyl)phenyl]-1,2,4-triazol-1-yl]-n'-pyrazin-2-ylprop-2-enehydrazide Chemical compound FC(F)(F)C1=CC(C(F)(F)F)=CC(C2=NN(\C=C/C(=O)NNC=3N=CC=NC=3)C=N2)=C1 DEVSOMFAQLZNKR-RJRFIUFISA-N 0.000 description 3
- ONBQEOIKXPHGMB-VBSBHUPXSA-N 1-[2-[(2s,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)propan-1-one Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1OC1=CC(O)=CC(O)=C1C(=O)CCC1=CC=C(O)C=C1 ONBQEOIKXPHGMB-VBSBHUPXSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 150000003863 ammonium salts Chemical class 0.000 description 3
- 229910052786 argon Inorganic materials 0.000 description 3
- 239000002775 capsule Substances 0.000 description 3
- 229940126142 compound 16 Drugs 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- DZGCGKFAPXFTNM-UHFFFAOYSA-N ethanol;hydron;chloride Chemical compound Cl.CCO DZGCGKFAPXFTNM-UHFFFAOYSA-N 0.000 description 3
- UREBWPXBXRYXRJ-UHFFFAOYSA-N ethyl acetate;methanol Chemical compound OC.CCOC(C)=O UREBWPXBXRYXRJ-UHFFFAOYSA-N 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 238000001953 recrystallisation Methods 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 description 3
- UAOUIVVJBYDFKD-XKCDOFEDSA-N (1R,9R,10S,11R,12R,15S,18S,21R)-10,11,21-trihydroxy-8,8-dimethyl-14-methylidene-4-(prop-2-enylamino)-20-oxa-5-thia-3-azahexacyclo[9.7.2.112,15.01,9.02,6.012,18]henicosa-2(6),3-dien-13-one Chemical compound C([C@@H]1[C@@H](O)[C@@]23C(C1=C)=O)C[C@H]2[C@]12C(N=C(NCC=C)S4)=C4CC(C)(C)[C@H]1[C@H](O)[C@]3(O)OC2 UAOUIVVJBYDFKD-XKCDOFEDSA-N 0.000 description 2
- STBLNCCBQMHSRC-BATDWUPUSA-N (2s)-n-[(3s,4s)-5-acetyl-7-cyano-4-methyl-1-[(2-methylnaphthalen-1-yl)methyl]-2-oxo-3,4-dihydro-1,5-benzodiazepin-3-yl]-2-(methylamino)propanamide Chemical compound O=C1[C@@H](NC(=O)[C@H](C)NC)[C@H](C)N(C(C)=O)C2=CC(C#N)=CC=C2N1CC1=C(C)C=CC2=CC=CC=C12 STBLNCCBQMHSRC-BATDWUPUSA-N 0.000 description 2
- IWZSHWBGHQBIML-ZGGLMWTQSA-N (3S,8S,10R,13S,14S,17S)-17-isoquinolin-7-yl-N,N,10,13-tetramethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-amine Chemical compound CN(C)[C@H]1CC[C@]2(C)C3CC[C@@]4(C)[C@@H](CC[C@@H]4c4ccc5ccncc5c4)[C@@H]3CC=C2C1 IWZSHWBGHQBIML-ZGGLMWTQSA-N 0.000 description 2
- UDQTXCHQKHIQMH-KYGLGHNPSA-N (3ar,5s,6s,7r,7ar)-5-(difluoromethyl)-2-(ethylamino)-5,6,7,7a-tetrahydro-3ah-pyrano[3,2-d][1,3]thiazole-6,7-diol Chemical compound S1C(NCC)=N[C@H]2[C@@H]1O[C@H](C(F)F)[C@@H](O)[C@@H]2O UDQTXCHQKHIQMH-KYGLGHNPSA-N 0.000 description 2
- HUWSZNZAROKDRZ-RRLWZMAJSA-N (3r,4r)-3-azaniumyl-5-[[(2s,3r)-1-[(2s)-2,3-dicarboxypyrrolidin-1-yl]-3-methyl-1-oxopentan-2-yl]amino]-5-oxo-4-sulfanylpentane-1-sulfonate Chemical compound OS(=O)(=O)CC[C@@H](N)[C@@H](S)C(=O)N[C@@H]([C@H](C)CC)C(=O)N1CCC(C(O)=O)[C@H]1C(O)=O HUWSZNZAROKDRZ-RRLWZMAJSA-N 0.000 description 2
- STPKWKPURVSAJF-LJEWAXOPSA-N (4r,5r)-5-[4-[[4-(1-aza-4-azoniabicyclo[2.2.2]octan-4-ylmethyl)phenyl]methoxy]phenyl]-3,3-dibutyl-7-(dimethylamino)-1,1-dioxo-4,5-dihydro-2h-1$l^{6}-benzothiepin-4-ol Chemical compound O[C@H]1C(CCCC)(CCCC)CS(=O)(=O)C2=CC=C(N(C)C)C=C2[C@H]1C(C=C1)=CC=C1OCC(C=C1)=CC=C1C[N+]1(CC2)CCN2CC1 STPKWKPURVSAJF-LJEWAXOPSA-N 0.000 description 2
- FHCCUFZRWVYQPM-UHFFFAOYSA-N 1,1'-biphenyl;hydrofluoride Chemical compound F.C1=CC=CC=C1C1=CC=CC=C1 FHCCUFZRWVYQPM-UHFFFAOYSA-N 0.000 description 2
- KKHFRAFPESRGGD-UHFFFAOYSA-N 1,3-dimethyl-7-[3-(n-methylanilino)propyl]purine-2,6-dione Chemical compound C1=NC=2N(C)C(=O)N(C)C(=O)C=2N1CCCN(C)C1=CC=CC=C1 KKHFRAFPESRGGD-UHFFFAOYSA-N 0.000 description 2
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- WZZBNLYBHUDSHF-DHLKQENFSA-N 1-[(3s,4s)-4-[8-(2-chloro-4-pyrimidin-2-yloxyphenyl)-7-fluoro-2-methylimidazo[4,5-c]quinolin-1-yl]-3-fluoropiperidin-1-yl]-2-hydroxyethanone Chemical compound CC1=NC2=CN=C3C=C(F)C(C=4C(=CC(OC=5N=CC=CN=5)=CC=4)Cl)=CC3=C2N1[C@H]1CCN(C(=O)CO)C[C@@H]1F WZZBNLYBHUDSHF-DHLKQENFSA-N 0.000 description 2
- UNILWMWFPHPYOR-KXEYIPSPSA-M 1-[6-[2-[3-[3-[3-[2-[2-[3-[[2-[2-[[(2r)-1-[[2-[[(2r)-1-[3-[2-[2-[3-[[2-(2-amino-2-oxoethoxy)acetyl]amino]propoxy]ethoxy]ethoxy]propylamino]-3-hydroxy-1-oxopropan-2-yl]amino]-2-oxoethyl]amino]-3-[(2r)-2,3-di(hexadecanoyloxy)propyl]sulfanyl-1-oxopropan-2-yl Chemical compound O=C1C(SCCC(=O)NCCCOCCOCCOCCCNC(=O)COCC(=O)N[C@@H](CSC[C@@H](COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)C(=O)NCC(=O)N[C@H](CO)C(=O)NCCCOCCOCCOCCCNC(=O)COCC(N)=O)CC(=O)N1CCNC(=O)CCCCCN\1C2=CC=C(S([O-])(=O)=O)C=C2CC/1=C/C=C/C=C/C1=[N+](CC)C2=CC=C(S([O-])(=O)=O)C=C2C1 UNILWMWFPHPYOR-KXEYIPSPSA-M 0.000 description 2
- MQISNDAUWVHJML-UHFFFAOYSA-N 1-butyl-4-fluorobenzene Chemical group CCCCC1=CC=C(F)C=C1 MQISNDAUWVHJML-UHFFFAOYSA-N 0.000 description 2
- WGFNXGPBPIJYLI-UHFFFAOYSA-N 2,6-difluoro-3-[(3-fluorophenyl)sulfonylamino]-n-(3-methoxy-1h-pyrazolo[3,4-b]pyridin-5-yl)benzamide Chemical compound C1=C2C(OC)=NNC2=NC=C1NC(=O)C(C=1F)=C(F)C=CC=1NS(=O)(=O)C1=CC=CC(F)=C1 WGFNXGPBPIJYLI-UHFFFAOYSA-N 0.000 description 2
- PYRKKGOKRMZEIT-UHFFFAOYSA-N 2-[6-(2-cyclopropylethoxy)-9-(2-hydroxy-2-methylpropyl)-1h-phenanthro[9,10-d]imidazol-2-yl]-5-fluorobenzene-1,3-dicarbonitrile Chemical compound C1=C2C3=CC(CC(C)(O)C)=CC=C3C=3NC(C=4C(=CC(F)=CC=4C#N)C#N)=NC=3C2=CC=C1OCCC1CC1 PYRKKGOKRMZEIT-UHFFFAOYSA-N 0.000 description 2
- TVTJUIAKQFIXCE-HUKYDQBMSA-N 2-amino-9-[(2R,3S,4S,5R)-4-fluoro-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-7-prop-2-ynyl-1H-purine-6,8-dione Chemical compound NC=1NC(C=2N(C(N(C=2N=1)[C@@H]1O[C@@H]([C@H]([C@H]1O)F)CO)=O)CC#C)=O TVTJUIAKQFIXCE-HUKYDQBMSA-N 0.000 description 2
- LFOIDLOIBZFWDO-UHFFFAOYSA-N 2-methoxy-6-[6-methoxy-4-[(3-phenylmethoxyphenyl)methoxy]-1-benzofuran-2-yl]imidazo[2,1-b][1,3,4]thiadiazole Chemical compound N1=C2SC(OC)=NN2C=C1C(OC1=CC(OC)=C2)=CC1=C2OCC(C=1)=CC=CC=1OCC1=CC=CC=C1 LFOIDLOIBZFWDO-UHFFFAOYSA-N 0.000 description 2
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- MDKXBBPLEGPIRI-UHFFFAOYSA-N ethoxyethane;methanol Chemical compound OC.CCOCC MDKXBBPLEGPIRI-UHFFFAOYSA-N 0.000 description 1
- 125000004705 ethylthio group Chemical group C(C)S* 0.000 description 1
- SMANXXCATUTDDT-QPJJXVBHSA-N flunarizine Chemical compound C1=CC(F)=CC=C1C(C=1C=CC(F)=CC=1)N1CCN(C\C=C\C=2C=CC=CC=2)CC1 SMANXXCATUTDDT-QPJJXVBHSA-N 0.000 description 1
- 229960000326 flunarizine Drugs 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 210000004907 gland Anatomy 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- JAXFJECJQZDFJS-XHEPKHHKSA-N gtpl8555 Chemical compound OC(=O)C[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N[C@H](B1O[C@@]2(C)[C@H]3C[C@H](C3(C)C)C[C@H]2O1)CCC1=CC=C(F)C=C1 JAXFJECJQZDFJS-XHEPKHHKSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 235000003642 hunger Nutrition 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- ZLVXBBHTMQJRSX-VMGNSXQWSA-N jdtic Chemical compound C1([C@]2(C)CCN(C[C@@H]2C)C[C@H](C(C)C)NC(=O)[C@@H]2NCC3=CC(O)=CC=C3C2)=CC=CC(O)=C1 ZLVXBBHTMQJRSX-VMGNSXQWSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- RENRQMCACQEWFC-UGKGYDQZSA-N lnp023 Chemical compound C1([C@H]2N(CC=3C=4C=CNC=4C(C)=CC=3OC)CC[C@@H](C2)OCC)=CC=C(C(O)=O)C=C1 RENRQMCACQEWFC-UGKGYDQZSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
- 125000006178 methyl benzyl group Chemical group 0.000 description 1
- 229940102396 methyl bromide Drugs 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-N methyl sulfate Chemical compound COS(O)(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-N 0.000 description 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 1
- PYLWMHQQBFSUBP-UHFFFAOYSA-N monofluorobenzene Chemical compound FC1=CC=CC=C1 PYLWMHQQBFSUBP-UHFFFAOYSA-N 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 230000004118 muscle contraction Effects 0.000 description 1
- 210000002464 muscle smooth vascular Anatomy 0.000 description 1
- 210000004165 myocardium Anatomy 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical group CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- LKPFBGKZCCBZDK-UHFFFAOYSA-N n-hydroxypiperidine Chemical compound ON1CCCCC1 LKPFBGKZCCBZDK-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 125000004923 naphthylmethyl group Chemical group C1(=CC=CC2=CC=CC=C12)C* 0.000 description 1
- IOMMMLWIABWRKL-WUTDNEBXSA-N nazartinib Chemical compound C1N(C(=O)/C=C/CN(C)C)CCCC[C@H]1N1C2=C(Cl)C=CC=C2N=C1NC(=O)C1=CC=NC(C)=C1 IOMMMLWIABWRKL-WUTDNEBXSA-N 0.000 description 1
- 230000000926 neurological effect Effects 0.000 description 1
- 230000000802 nitrating effect Effects 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N p-toluenesulfonic acid Substances CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 210000005259 peripheral blood Anatomy 0.000 description 1
- 239000011886 peripheral blood Substances 0.000 description 1
- 239000000810 peripheral vasodilating agent Substances 0.000 description 1
- 229960002116 peripheral vasodilator Drugs 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 229960003742 phenol Drugs 0.000 description 1
- XZTCTKKANUDQCW-UHFFFAOYSA-N piperamine Natural products C=1C=C2OCOC2=CC=1CCC=CC(=O)N1CCCC1 XZTCTKKANUDQCW-UHFFFAOYSA-N 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- 125000004742 propyloxycarbonyl group Chemical group 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 150000003385 sodium Chemical class 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- NVIFVTYDZMXWGX-UHFFFAOYSA-N sodium metaborate Chemical compound [Na+].[O-]B=O NVIFVTYDZMXWGX-UHFFFAOYSA-N 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010408 sweeping Methods 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- DDFYFBUWEBINLX-UHFFFAOYSA-M tetramethylammonium bromide Chemical compound [Br-].C[N+](C)(C)C DDFYFBUWEBINLX-UHFFFAOYSA-M 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 239000008215 water for injection Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
- C07D295/084—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/088—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/06—Antiarrhythmics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/125—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/13—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Cardiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Heart & Thoracic Surgery (AREA)
- General Health & Medical Sciences (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Description
s'82 isrJA. κ;··νΊ—.——
Rt 五 技 哌 基 苯二 的 穎 新 之 用 作 抗 拮 0 力 強 有 具 於 ) 關 (1為 明域明 説領發 Σ術本 之 患 疾 統 条 琿 循 ΒΒΒ 各 於 用 利 可 0 其蕖 含用 及器 ,環 鹽循 其的 或防 物預術 生及技 衍療景 啡治背 物阻 藥為 種蕖 種抗 的拮 的0 目 , 防中 預其 和 〇 療用 治使 之之 病上 疾床 統睡 条以 環供 循被 以並 ,發 往開 以被 已 ί請先間4背而之注-苹項再塡寫本頁) 裝 止心肌和血管平滑肌之細胞膜興奮所伴隨的鈣離子往細 胞内之特異的流入,並抑制肌肉收縮且擴張血管。因此 ,0拮抗藥因其有用於高血壓,狹心症,腦血流瘅礙等 之治療及預防而被注意[Pharmacological Reviews. 38 ( 4 ) , 32 卜 4 1 6 ( 1 9 86 ) ] 〇 訂 如此的鈣拮抗藥之代表例,雖於臨床應用被做為腦循 環改善藥有氰苯桂哄(flunarizine) [Journal of the neurological Science. 25, 371-375(1975)]和於臨床應 用被做為末梢血管擴張劑有肉桂苯掀拼(cinnarizine) [Drugs of today. 18. 27〜42(1982)]但仍期望新穎的 副作用少具有鈣拮抗作用藥剤之開發。 因此,本發明之目的為提供具有優異鈣拮抗作用且可 做為B藥之新穎化合物,及含其之循琛器用藥。 經濟部中央標準局8工消費合作杜印製 在這樣的事實下,本發明者精心研究結果發現後述以 式(I)所表示之新穎的二苯基哌畊衍生物或其鹽具有比 以往所使用之《苯桂哄和肉桂苯岍畊更強的鈣拮抗作用 ,且毐性低安全性高,可廣為利用做為循琛器用藥,因 而完成本發明。 發明之掲示 -3 -本紙張尺度通用中阀阀家標準(CNS)甲4规格(210 X 297公釐) Λ6 136 五、發明説明(2 ) 本發明為提供下式(1)所代表之二苯基哌阱衍生物或 其鹽做為循環器用藥之有效成分。
〔式中 烷基, 三氟甲 或可被 基.芳 基,可 ,R1及R2可相同或相異各為氫原子,鹵原子, 烷氧基,硝基,胺基,羥基,可被酯化之羧基或 基,R3為氫原子,烷基,芳烷基,醯基,硝基 酯化之羧甲基,Ar為1〜3個鹵原子,烷基,烷氧 氣基,芳烷氣基,硝基,胺基,氰基,醯基,羥 被酯化之羧基,被取代磺醯基,芳基,可被取代 (請先閱讀背面之注意事項再填寫本頁) 裝. 經濟部屮央標準局貝工消費合作社卬製 以苯基或萘基之三氟甲基,Z為硫原子或-N-(R4為氫原 子,烷基,芳烷基,醯基,芳基,被取代磺醯基或可被 醋化之羧基),m為1〜5之整數,η為0〜5之整數〕 實施本發明之最佳狀況 上述式(1)中,鹵原子可列舉氟原子,氛原子,碘原 子,溴原子等,而烷基可列舉甲基,乙基,丙基,異丙 基,丁基,異丁基,第二丁基,第三丁基,戊基,異戊 基,新戊基,己基,辛基,壬基,癸基,環苄基,環己 基等之磺數為1〜10者,烷氧基可列舉甲氣基,乙氣基 ,丙氣基,異丙氣基,丁氧基,苄氧基,己氧基,環苄 4 - 本紙張尺度逍用中國Η家標準(CNS)甲4規格(210X297公*) 經濟部中央標準局貝工消費合作社製 ^050〇^ Λ 6 _Β6_ 五、發明説明(3 ) 氧基,環己氧基等之碩數為1〜8者,而可被酯化之羧基 可列舉甲氧羰基,乙氧羰基,丙氧羰基,丁氣羰基等之 烷氣羰基·,可被酯化之羧甲基可列舉甲氧羧甲基,乙氣 羰甲基,羧甲基等。又,芳烷基可列舉苄基,苯乙基, 甲苄基,萘甲基等,醯基可列舉乙醯基,丙醯基,丁醯 基等之烷醯基和苄醯基,鹵苄醯基,烷氣苄醛基等之芳 醯基等,芳基可列舉具有1個以上取代基之苯基(取代 基種類可列舉鹵素,烷基,烷氣基,羥基,胺基等)等€ 芳氧基可列舉苯氣基等,芳烷氧基可列舉苄氣基,取代 礎醯基可列舉甲烷磺醯基,對甲苯磺醯基等。 若於此類基中列舉持佳者則R1及R2為氫原子或鹵原 子,R3為氫原子,烷基,烷醯基,硝基或苄基。 又,做為二苯基哌阱衍生物(1)之鹽若做為醫藥之容 許鹽則無待別限制,例如可為酸加成鹽及第4级銨鹽。 用以酸加成鹽形成之酸可為有機酸或無機酸,有機酸可 列舉醋酸,反丁烯二酸.順丁烯二酸,檸樣酸,丙二酸 ,甲烷磺酸,對甲苯磺酸等之磺酸類等,無機酸可列舉 鹽酸,硫酸,硝酸,磷酸,硼酸等。又,用以第4级銨鹽 形成之化合物可列舉甲基氯,甲基溴,甲基碘之烷基鹵 甲換硫酸,二甲換硫酸等之烷基硫酸等。 這些二苯基哌阱衍生物(1)之特佳具體例可列舉出下 列化合物及其鹽。 • 1-二苯甲基- 4-(2-羥基-3-苯硫丙基)哌阱 -5 - (請先閲讀背面之注意事項再填寫本頁) 裝· 各紙張尺度遑用中a B家樣毕(CNS)甲4規格(210><297公龙) 經濟部中央標準局貝工消費合作社卬製 Λ 6 _Β6_ 五、發明説明(4) • 1-〔 4, 4-雙(4-氟苯基)丁基〕-4-(2-羥基-3-苯硫丙 基)哌阱 • 1-〔 4,4-雙(4-氟苯基> 丁基〕-4-(2 -甲氧基-3-苯硫 丙基)哌阱 0 • 1-(2-乙醯氧基-3-苯硫丙基)-4-〔4,4-雙(4-氟苯基) 丁基〕呢阱 • (S)-(-)-l-〔4,4-雙(4-氟苯基)丁基〕-4-(2-羥基-3 -苯硫丙基)哌阱 • ( R ) - ( + ) - :1 -〔 4 , 4 -雙(4 -氟苯基)丁基]-4 - (2 -羥基-3 -苯硫丙基)哌阱 • 1-〔 4,4-雙(4-氟苯基)丁基〕-4-(2-羥基-3-(4 -甲基 苯硫基)丙基〕哌畊 • 1-(2-羥基- (4-胺苯硫基)丙基〕-4-〔4,4-雙(4-氟苯 基)丁基]呢阱 • 1-〔雙(4-氟苯基)甲基〕-4-(2-羥基-3-苯甲硫丙基) 哌阱 • 1-〔 3,3-雙(4-氟苯基)丙基〕-4-(2-羥基-3-苯硫丙 基)呢阱 • 1-〔 4,4-雙(4-氟苯基)丁基〕-4-(2-羥基-3-苯甲硫 丙基)哌阱 • 1-〔4,4 -雙(4 -氟苯基)丁基〕-4-〔 3-(4 -氮苯硫基)-2-羥丙基〕哌阱 • 1-〔4, 4-雙(4-氟苯基)丁基〕-4-〔 3-(3,4-二氣苯硫 各紙張尺度遑用中B國家標準(CNS)甲4規格(210x297公*) (請先閲讀背面之注意事項再填寫本頁) 裝· 訂. Λ 6 Β6 五、發明説明(5 ) 基)-2-羥丙基〕哌阱 • 1-〔 4,4-雙(4-氣苯基)丁基〕-4-〔2-羥基-3-(2-甲 氧苯硫基)丙基〕哌阱 • 1-〔4,4-雙(4-氟苯基)丁基〕-4-〔 3-(4-氣苯硫基)-2-羥丙基〕哌阱 • 1-〔 4,4-雙(4-氣苯基)丁基〕-4-(2-羥基- 3-(4-羥苯 硫基)丙基)哌阱 • 1-〔 4,4-雙(4-氣苯基)丁基〕-4-(2-羥基- 3-(4 -甲氣 苯硫基)丙基)哌阱 • 1-〔 4,4-雙(4-氟苯基)丁基〕-4-(2-羥基- 3-(3-甲氣 苯硫基)丙基)哌阱 •卜〔雙(4-氟苯基)甲基〕-4-(2-羥基-3-(2-甲氣苯硫 基)丙基)哌阱 • 1-〔2,2-二苯乙基)-4 -(2-羥基-3-苯硫丙基)瞰阱 • 1-〔3,3-二苯丙基)-4-(2-羥基-3-苯硫丙基)呢阱 • 1-〔 4,4-二苯丁基)-4-(2-羥基-3-苯硫丙基)哌阱 • 1-〔雙(4-氟苯基)甲基〕-4-(2-羥基-3-苯硫丙基)哌 阱 - 經濟部中央標準局员工消費合作社卬製 (請先閲讀背面之注意事項再填寫本頁) • 1-〔雙(4-氟苯基)甲基]-4-〔2-羥基- 3-(4 -甲氣苯 硫基)丙基〕派阱 • 1_〔 4, 4 -雙(4 -氣苯基)丁基〕-4-〔 2 -翔基- 3- (1-策 硫基)丙基]哌阱 ♦1-C 4,4-雙(4-氟苯基)丁基〕-4-〔2-羥基- 3-(2,3,4 -7 - 各紙張尺度逍用中困國家標準(CHS)甲4規格(210x297公*) Λ 6 Β6 經濟部中央標準局員工消費合作社卬製 五、發明説明(6 ) -三甲氧苯硫基)丙基〕哌阱 • 1-〔4, 4-雙(4-氟苯基)丁基〕-4-〔 3-(3,4-二甲氣苯 硫基)-2-羥丙基〕哌阱 • 1-〔 4,4-雙(4-氟苯基)丁基〕-4-〔2-羥基- 3-(3,5-二-第三丁基-4-羥苯硫基)丙基〕哌阱 • 1-二苯甲基- 4- (2 -羥基-3-苯甲硫丙基)哌阱 • 1-二苯甲基- 4-(2-羥基-3-(2-苯乙硫基)丙基)哌畊 •卜二苯甲基-4-〔2 -經基-3- (2-( 2 -甲氧苯基)乙硫基)丙 基〕哌阱 •1-〔3- (2-(3,4-二甲氣苯基)乙硫基} -2-羥丙基〕 -4 -二苯甲基哌阱 • 1-〔 4, 4-雙(4-氟苯基)丁基〕-4-〔2-羥基-3-(2-苯 乙硫基)丙基〕哌阱 • 1-〔 4,4-雙(4-氣苯基)丁基]-4-(2-硝氣丙基-3-苯 硫基)哌阱 • 1-〔 4,4-雙(4-氟苯基)丁基]-4-(2-苄氣丙基-3-苯 硫基)哌阱 ♦1-〔4,4-雙(4-氟苯基)丁基]-4-〔2-羥基-3-(4-硝 苯硫基)丙基〕哌阱 ·]-〔 4,4-雙(4-氟苯基)丁基〕-4-〔2-羥基- 3-(3-苯 丙硫基)丙基〕哌阱 • 1- [4 ,4-雙(4-氟苯基)丁基〕-4- [3-(4-氱苯甲硫基 )-2-羥丙基〕呢阱 -8 - (請先閲讀背面之注意事項再填寫本頁) 本紙張尺度逍用中國困家標準(CNS)甲4規格(210x297公*) 050ΰ^ A 6 B6 五、發明説明(7) 雙 基 丁 V)- 基 苯 氣 甲 苯 氣二 基 硫 羥 基 硫 甲 苯 基 基 硫 甲 苯 氣 2- \1/ 基 硫 甲 基 ^ 丙 1 丙 丙雙 > 雙}雙羥雙 基 基 阱 哌 氟 氟 氟 基阱基畊基 苯哌苯哌苯 基 基 基 丁 阱 哌 J 基 丙 基 苯 氟 基 羥 基 羥 甲 甲 苯 氧 甲二 基 硫 甲 苯 氧 甲 三
基雙 甲 4 苯4, 二 C 3 基 基羥 丙2- 基阱 丁哌 基 羥 丙 胺 苯 I 3 1 阱基 哌羥 基(2 丙4- 胺)- -«* 丁 \1/ 基 苯 氟 (請先閲讀背面之注意事項再填寫本頁) 裝. 阱 哌 \ly 基 基 苯 氟 I 4 /V 雙 哌 J 基 丙 基 胺 苯 I N 基 甲 基 醯 乙 基 胺 基 I 丙 (4胺(4氧 雙苯雙甲 4 Η 4 ^ 氟 氟 基基基 ^ έ. tTT 0r 基 哌 基 基阱基 丁 阱丁哌 丁阱 基 氣 甲 基 氧 醯 乙 苯 f N 1 基 甲 訂- 經濟部中央標準局貝工消費合作社卬製 阱 哌 基 丙 胺 苯 阱 哌 基 丙 胺 苯 基 丁 基 苯 氟- 4 /IV 雙 基 羥 雙 基 丁 基 苯 氣 3- 基 羥 9 本紙張尺度適用中Β國家標準(CNS)甲4規格(210X297公釐) A 6 Β6 經濟部中央標準局貝工消費合作社印?反 五、發明説明(8 ) • 1-〔 4, 4-雙(4-氟苯基)丁基〕-4-〔2-羥基- 3-(4-甲 苯胺基)丙基〕哌阱 • 1-〔(4-胺基苯胺基)-2-羥丙基〕-1-〔4,4-雙(4-氟 苯基)丁基]哌阱 •1-〔雙(4-氟苯塞)甲基〕-4-(2-羥基-3-苯甲胺丙基 )哌阱 • 1-〔 3,3-雙(4-氟苯基)丙基〕-4-(2-羥基-3-苯胺丙 基)哌阱 • 1-〔 4,4-雙(4-氟苯基)丁基〕-4-(2-羥基-3-苯甲胺 丙基)哌阱 • 1-〔 4,4-雙(4-氟苯基)丁基〕-4-〔 3-(4-氛苯胺基) -2-羥丙基]哌阱 • 1-〔4,4-雙(4-氟苯基)丁基〕-4- [3-(3,4-二氮苯胺 1 基)-2-羥丙基〕哌阱 • 1-〔 4, 4-雙(4-氟苯基)丁基〕-4-〔2-羥基- 3-(2-甲 氣苯胺基)丙基〕哌阱 • 1-〔4,4-雙(4-氟苯基)丁基〕-4-〔 3-(4-氟苯胺基) -2-羥丙基〕哌胼 • 1-〔 4,4-雙(4-氟苯基)丁基〕-4-(2-羥基- 3-(4-羥苯 胺基)丙基)哌阱 ♦1-〔 4,4-雙(4-氟苯基)丁基〕-4-(2-羥基- 3-(4-甲氣 苯胺基)丙基)哌阱 • 1-〔 4,4-雙(4-氟苯基)丁基〕-4-(2-羥基- 3-(3-甲氣 -10- (請先閲讀背面之注意事項再填窝本頁) 裝· 訂· · ·.線· f 本紙張尺度逍用中困國家標準(CNS)甲4規格(210x297公*) 〇5〇ύ a A 6 B6 五、發明説明(9 ) 阱 哌 \1/ 基 丙 基 胺 苯 基 丁 \ϊ/ 基 苯 氟 1 4 fv 雙 苯 I 3 I 基 氧 醯 乙 阱 哌 基 丙 胺 - - -* 4 4 4 I I I ιφ \Ί/ νϊ/ \—/ 基基基基 乙丙丁苯 苯苯苯氟二二二4- I I I { 2’ 3’ 4,雙 +U ^ ^ 令 τ^為 I I I 3 3 3 I I _ 基基基 0 0 0 基 羥 基基基苯 丙丙丙3-胺 胺胺· 阱胼阱 哌哌哌 呢 \1/ 基 丙 胺 阱 雙 丙 \ly 基 胺 丙 \i/· 基 胺 雙t雙 I—- _ i—N I 基,4基,4 基 甲 \1/ 基 苯阱 氟哌 基 丁 基 苯 氟 阱 哌 基 丁 基 苯 氟 肼 哌 基 丙 基 胺 苯 氣 甲三 基 胺 3基3 雙丙雙 4-經4- 基 丁 基 苯 氟 阱 哌 基 丁 基 丙 羥 基2-苯)-氟基 4-胺 /IV 苯 基 丁三 第-二 基 羥 基 羥 基 羥 苯 氧 甲 萘 苯 氧 甲二 基 羥 (請先閲讀背面之注意事項再填寫本頁) 經濟部屮央標準局員工消費合作杜.卞製 基基基 甲 甲 甲 f fft tTT τ2* 阱 哌 *—s 基 丙 苯- 3 I 基 丙 羥- 2 基基 羥羥 基胺甲 畊胺乙2-哌甲苯-( 哌 基氣 基 阱丙 基 苯 阱基 哌胺 I—·> 乙 基 胺 乙 SJ/ 基 苯 氧 甲 基 丙 羥 本紙張尺度逍用中困國家標毕(CNS)甲4規格(210X297公龙) 經濟部中央標準局員工消f合作社卬吸 S〇5〇 把A 6 _B6_ 五、發明説明(10) 4-二苯甲基哌阱 • 1-〔4,4 -雙(4 -氟苯基)丁基〕-4-〔2 -羥基-3-(2 -苯 乙胺基)丙基〕哌阱 • 1-〔4,4-雙(4-氟苯基)丁基〕-4-〔2-羥基- 3-(4-硝 苯胺基)丙基〕哌阱 • 1-〔4,4-雙(4-氟苯基)丁基〕-4-〔2-羥基- 3-(3-苯 丙胺基)丙基〕哌阱 • 1-〔 4,4-雙(4-氟苯基)丁基〕-4-〔 3-(4-氣苯甲胺基 )-2-羥丙基〕哌阱 • 1-〔 4, 4-雙(4-氟苯基)丁基〕-4-〔 3-(3,4-二氛苯甲 胺基)-2-羥丙基〕哌畊 • 1-〔4,4-雙(4-氣苯基)丁基]-4-〔2-羥基- 3-(4 -甲 基苯甲胺基)丙基〕哌阱 • 1-〔4, 4-雙(4-氟苯基)丁基〕-4-〔2-羥基- 3-(4 -甲 基苯甲胺基)丙基〕哌阱 • 1-〔4,4-雙(4-氟苯基)丁基〕-4-〔 3-(2,3-二甲氧苯 甲胺基)-2-羥丙基〕哌阱 • 1-〔4,4-雙(4-氣苯基)丁基〕-4-〔2-羥基- 3-(2 ,3, 4 -三甲氣笨甲胺基)丙基〕哌阱 •1-〔4,4-雙(4-氟苯基)丁基]-4-〔2-羥基-3-([^-甲基 -N-苯胺基)丙基〕哌阱 • 1-〔4,4-雙(4-氟苯基)丁基〕-4-〔2-羥基- 3-(N-苯基 -N-苯甲胺基)丙基〕哌阱 -1 2 - (請先閲讀背面之注意事項再填寫本頁) 裝· 訂_ 本紙張尺度逍用中困困家標準(CNS)甲4規格(210X297公釐) 經濟部中央標準局貝工消費合作社·^¾ Α6 _Β6_ 五、發明説明(11) .-乙醯基-Ν-苯胺基)-2 -羥丙基〕-4ί 4 , 4 -雙(4 -氟苯基> 丁基〕哌阱 ♦1-〔4,4-雙(4-氟苯基)丁基〕-4-〔3-(^1-乙氣羰基-[< -苯胺基)-2-羥丙基〕哌阱 •卜〔4,4-雙(4-S 苯基)丁基〕-4-〔3-(N,N-二苯胺基 )-2-羥丙基〕哌阱 • 1-〔4,4-雙(4-氟苯基)丁基〕-4-〔2-羥基-3-(N-甲 磺醯基-N-苯胺基)丙基〕哌阱 •1-〔4,4-雙(4-氟苯基)丁基〕-4-〔2-羥基-3-{卜(4 -甲苯基)磺醯基-N-苯胺基)丙基〕哌阱 • 1-〔 4,4-雙(4-氟苯基)丁基〕-4-〔 2-乙氣羰甲氣基-3-苯硫丙基〕呢阱 .1-苯硫甲基-2-〔4-(4,4-雙(4-氟苯基)丁基〕哌畊基 〕乙氣醋酸納 本發明化合物(1)或其鹽,例如可遵從下列反應式以 常法製得。 (譆先閲讀背面之注意事項再填寫本頁) 裝- 訂_ 線_ -13- 木紙張尺度逍用中國國家標準(CNS)甲4規格(210X297公釐)
66 AB 五、發明説明(I2)
CmH 8 m- Γ~~\ / \ •N N-CH3CH-CHa + HZ-C„HSn-Ar (2) (3)
NH + CHa-CHCH3-Z-CnH8n-Ar (4) 5) (請先閲讀背面之注意事項再填寫本頁)
OH r~\ I CnHam-,-Ν N-CH3CHCHa-Z-CnHSn-Ar (la) 裝· 訂一 \t OR: C«Ham-i-N N-CHaCHCHj-Z-CnHan_Ar \__f (lb) 線· 經濟部中央標準局貝工消費合作社印製 〔式中,R1 ,R2 ,R3 ,Z,m及n同前定義〕 即,藉由化合物(2)與化合物(3)使於鹼性觸媒存在或 不存在之溶劑中,室溫或加熱下反應,或藉由化合物(4) 與化合物(5 )使於溶劑中室溫或加熱下反應,可取得R 3 為氫原子之本發明化合物(la),其次若使於烷化劑,芳 烷化劑,醯化劑或硝化劑中反應,則可取得R 3為烷基, 芳烷基,醯基或硝基之本發明化合物(lb)。 •14- 本紙張尺度逍用中B國家標準(CNS)甲4規格(210X297公《) A 6 B6 五、發明説明(13) 硝基之本發明化合物(1 b )。 於化合物(2)與化合物(3)反應中所使用之鹼性觸媒可 列舉碩酸鈣,磺酸納等。 又,化合物(2 )與化合物(3 )之反應,或化合物(4 )與 化合物(5)之反應中所使用之溶劑可列舉低级醇,二甲 基甲醯胺(以下簡稱「DMF」)等。 反應化合物(la)之試劑可列舉烷基鹵或芳烷基鹵與強 鹼之組合,醯基鹵,酸酐-毗啶,醋酸酐-濃硝酸溶液等 〇 又,化合物(1)中被酯化羧基或羧甲基取代基存在之 情形時,可藉由常法以水解使其酯殘基被脱離。做為所 得本發明化合物(1 )之鹽可依一般胺基化合物酸加成鹽之 調製法,第4级銨鹽之調製法進行,例如當於酸加成鹽 , 之調製,若於化合物(1)之有機溶劑溶液中加入酸亦可。 由此所得之本發明化合物(1)或其鹽之粗製産物若以 再結晶,薄層靥析,柱層析,急驟層析,分取高速液體 層析等精製,則可取得本發明化合物(1 )或其鹽之純化 物。 經濟部中央標準局員工消費合作社.--11製 (請先閲讀背面之注意事項再填寫本頁) 如上述所取得之本發明化合物(1)為具有優異的鈣拮 抗作用,且安金性亦高,可做為循環器用藥,利用於種 種疾病之預防或治療。 本發明之循環器用藥為以本發明化合物(1)之一種或 二種以上之混合物做為有效成分,且將此混合以液體或 -1 5 - 各紙張尺度逍用中國困家標準(CNS)甲4規格(210x297公龙) L030c;4 Λ 6 B6 經濟部中央標準局员工消費合作杜·-f製 五、發明説明(14) 固體之製劑補助成分,例如賦形劑,結合劑,稀釋劑, 並以粉末,顆粒,錠劑,膠囊,液劑,注射劑等任意之 劑形可經口或非經口的投予。 投予量雖依年齡,體重,症狀而適量增減,但成人1 天經口投予化合物(1)之場合,較佳為10〜1000毫克。 亦可將1天投予量不需1次投予而分成數回投予。又, 不用說亦可調合以其他必要之藥劑並投予。 實施例 其後所列舉之實施例及試驗例為更詳細說明本發明, 但本發明並不侷限於此實施例中。 實施例1 卜二苯甲基- 4- (2 -羥基-3-苯胺丙基)哌阱(化合物1): 3.08克(0.01莫耳)之1-(二苯甲基)-4-(2 ,3-環氧丙基 )哌阱與0.93克(0.01莫耳)之苯胺於觸媒量碩酸鈣等之 驗存在下,與200毫升DMF共同加熱迴流21小時,並於減 壓蒸除DHF後,以乙酸乙酯萃取殘渣,水洗,乾燥後減 壓蒸除乙酸乙酯,可得4克黏稠性液狀之粗製標的化合 物。關於此之急驟層析及分取之薄層層析於乙酸乙酯甲 醇混合溶劑条統及二氱甲烷♦甲醇混合溶劑条統下進行 ,可得2克黃色結晶狀之精製的標題化合物。 1 H-NMR 光譜(δ ppm): 2.3-2.7(m,10H),3.0-3,l(m,lH),3.2-3,3(ni,lH), 3.9-4.0(m,lH),4.2(s,lH),6.6-6.8(m,5H), -16- (請先閲讀背面之注意事項再填寫本頁) 裝. 訂. 本紙張尺度逍用中國Η家標準(CNS)甲4規格(210乂297公龙) Λ 6 B6 五、發明説明(15) 7.1- 7.5(ηι,10Η) 質譜 402 (Μ + Η) IR光譜 3400,2800,1600,1 500,1150 cm'1 熔點:1 58 - 1 60 1 實施例2 1-二苯甲基- 4-(2-羥基-3采甲胺丙基)哌阱(化合物2): 3.08克(0.01莫耳)之1-(二苯甲基)-4-(2,3-環氧丙基 )哌阱與1克(0.01莫耳)之苄胺於觸媒量磺酸鈣等之鹼 存在下,與200毫升DMF共同加熱迴流5小時,並於減壓 蒸除DHF後,以乙酸乙酯萃取殘渣,水洗,乾燥後減壓 蒸除乙酸乙酯,可得4.8克黏稠性液狀之粗製標的化合 1 物。關於此之急驟層析及分取之薄層層析於乙酸乙酯甲 醇混合溶劑条統及二氯甲烷•甲醇混合溶劑条統下進行 ,可得1.2克ή色結晶狀之精製的標題化合物。 1 H-NMR 光譜(δ ρρβ): 2.2- 2.7(m,12H),3.7-3.9(m,3H),4.2(s,lH), 7.1-7.5 (m, 15H) 經濟部中央標準局員工消費合作杜印製 (請先閲讀背面之注意事項再填寫本頁) 質譜 416 (M + H ) IR光譜 3400,2800,1600,1500,1150 cm*1 -17- 本紙張尺度逍用中8國家標毕(CNS)甲4規格(210X297公*) A 6 B6 S050S4 五、發明説明(16) 熔點:76 - 80 1 實施例3 卜二苯甲基-4-〔2 -羥基-3-苯乙胺)丙基〕)哌阱(化 合物3 ): 3.08克(0.01莫耳)之1-(二苯甲基)-4-(2,3-*環氧丙基 )哌阱與1.2克(0.01莫耳)之2 -苯乙胺於觸媒量碩酸鈣 等之鹼存在下,與200毫升DMF共同加熱迴流24小時,並 於減壓蒸除DMF後,以乙酸乙酯萃取殘渣,水洗,乾燥 後減壓蒸除乙酸乙酯,可得5克黏稠性液狀之粗製標的 化合物。關於此之急驟層析及分取之薄層層析於乙酸乙 酯甲醇混合溶劑糸統及二氣甲烷♦甲醇混合溶劑糸統下 進行,可得1.5克白色結晶之精製的標題化合物。 1 Η - H M R 光譜(δ p p m ): 2.2-2.9(m,16H),3.7-3.85(m,lH),4.2(s,lH), 7.1-7.45 (m,15H) 質譜 430 (M + H) IR光譜 3400,2800,1600,1500,1150 cm'1 焰點:11 4 - 11 5 1C 實施例 4 1-二苯甲基- 4- (2 -羥基-3- {2-(2 -甲氣苯基)乙胺基} 丙基〕呢阱(化合物4): 一 1 8 _ 本紙張尺度通用中國困家標準(CNS)甲4規格(210x297公*) (請先閲讀背面之注意事項再填寫本頁) 裝· 訂_ 經濟部屮央標準局員工消費合作社卬製 經濟部屮央標準局员工消费合作社卬製 A 6 _Β6_ 五、發明説明(17) 3.08克(0.01莫耳)之1-(二苯甲基)-4-(2,3 -環氧丙基 )哌阱與2克(0.01莫耳)之2-(2 -甲氧苯基)乙胺於觸媒 量之磺酸鈣等之鹼存在下,與200毫升DMF共同加熱迴流 21小時,並於減壓蒸除DMF後,以乙酸乙酯萃取殘渣, 水洗,乾燥後減壓蒸除乙酸乙酯,可得5.1克黏稠性液 狀之粗製標的化合物。關於此之急驟層析及分取之薄層 層析於乙酸乙酯·甲醇混合溶劑糸統及二氣甲烷•甲醇 混合溶劑条統下進行,可得3.05克黏稠性液狀之精製的 標題化合物。 1 H-NMR 光譜(δ ppm): 2.2-2.9(m,16H),3.8-3.9(m,4H),4.2(s,lH), 6.75-6.85 (m,2H),7,;l-7.4(m,12H) 質譜 ,. 460 (M + H ) IR光譜 3400,2800,1600,1500,1150 cm-1 實施例5 1-〔3-{2-(3,4-二甲氧苯基)乙胺基}-2-羥丙基] -4 -二苯甲基哌阱(化合物5): 3.08克(0.01莫耳)之1-(二苯甲基)-4-(2 ,3-環氧丙基 )呢阱與2克(0.01莫耳)之2-(3,4-二甲氣苯基)乙胺於 觸媒量之碩酸鈣等存在下,與200毫升DMF共同加熱迴流 2 4小時,並於減壓蒸除D M F後,以乙酸乙酯溶劑萃取殘 -1 9 - 本紙張尺度逍用中國國家標準(CNS)甲4規格(210x297公龙) (請先閲讀背面之注意事項再填寫本頁) 裝· 訂_ Λ 6 Β 6 經濟部中央標準局員工消費合作社印製 五、發明説明(18) 渣,水洗,乾燥後減壓蒸除乙酸乙酯,可得5.1克黏稠 性液狀之粗製標題化合物。關於此之急驟層析及分取之 薄層層析於乙酸乙酯·甲醇混合溶劑条統及二氣甲烷•甲 醇混合溶劑糸統下進行,可得1.2克黏稠性液狀之精製 的標題化合物。 1 H-NMR 光譜(5 ppm): 2.2-2.9U,16H),2.7-3.85(m,7H),4.2(s,lH), 6.7-6.85(m,2H),7.1_7.4(ro,llH) 質譜 490 (M + H ) IR光譜 3400,2800,1600,1500,1150 cm'1 實施例6 1-〔4,4-雙(4-氟苯基)丁基〕-4-(2-羥基-3-苯胺丙 基)哌阱(化合物6 ): 3.86克(0.01莫耳)之1-〔4,4-雙(4-氟苯基)丁基〕-4-(2 ,3 -環氧丙基)哌阱與0.93克(0.01莫耳)之苯胺於觸媒 量之碩酸鈣等之驗存在下,與200毫升DMF共同加熱迴流 2 1小時,並於減壓蒸除D M F後,以乙酸乙酯溶劑萃取殘 渣,水洗,乾燥後減壓蒸除乙酸乙酯,可得5克黏稠性 液狀之粗製標題化合物。關於此之急驟層析及分取之薄 層層析於乙酸乙酯·甲醇混合溶劑条統及二氯甲烷•甲醇 混合溶劑条統下進行,可得0.5克黏稠性液狀之精製的 (請先閲讀背面之注意事項再填寫本頁) 裝· 本紙張尺度遑用中a a家樣毕(CNS)甲4規格(210X297公«:) 經濟部中央標準局員工消費合作社印製 A 6 B6 五、發明説明(1彡 標題化合物。 1 H-NMR 光譜(δ ppm): 1.3- 1.5(ra,2H),1.9-2.1(m,2H),2.2-2.8U,12H), 2.95-3.1(πι,1Η),3.1-3.3(πι,1Η),3.8-4(πι,2Η), 6.5-6.75(m,5H),6·8-7.2(η,8Η) 質譜 480 (Μ + Η) IR光譜 3400,2800,1600,1500,1150 cm'1 實施例7 1-〔 4,4-雙(4-氟苯基)丁基〕-4-(2-羥基-3-苯甲胺 丙基)哌阱(化合物7): 3.86克(0.01莫耳)之卜〔4,4-雙(4-氟苯基)丁基〕-4-(2,3-環氧丙基)哌阱與1克(0.01莫耳)之苄胺於觸媒量 之磺酸鈣等之鹼存在下,與200毫升DMF共同加熱迴流24 小時,並於減壓蒸除DMF後,以乙酸乙酯溶劑萃取殘渣 ,水洗,乾燥後減壓蒸除乙酸乙酯,可得5克黏稠性液 狀之粗製標題化合物。關於此之急驟層析及分取之薄層 層析以乙酸乙酯·甲醇混合溶劑条統及二氱甲烷♦甲醇混 合溶劑糸統進行,可得0.5克黏稠性液狀之精製的標題 化合物。 ^ 1 Η - N M R 光譜(δ p p m ): 1.3- 1.5(ηι,2Η),1.9-2(ιπ,2Η),2.1-2.7(ιβ,12Η), 本紙張尺度逍用中國困家標準(CNS)甲4規格(210X297公釐) (請先閲讀背面之注意事項再填寫本頁) 裝- A 6 _B6_ 五、發明説明fe〇) 3-3.15(m,2H),3.75-3.9(m,2H),4.55(s,2H), 6.8- 7 (m,5H),7-7.4(m,8H) 質譜 49 4 (M + H) ' IR光譜 3400,2800,1600,1500,1150 cm'1 實施例 8 1-〔4,4-雙(4-氟苯基)丁基〕-4-(2-羥基- 3-(2-苯乙 胺基)丙基〕哌阱(化合物8): 3,86克(0,01莫耳)之1-〔4,4-雙(4-氟苯基)丁基〕Μα,3-環氣 丙基) 哌阱與 1.2 克 (0.01 莫耳) 之 2-苯 乙胺於 觸媒量之磺酸鈣等之鹼存在下,與200毫升DMF共同加熱 迴流24小時,並於減壓蒸除DMF後,以乙酸乙酯溶劑萃 取殘渣,水洗,乾燥後減壓蒸除乙酸乙酯,可得5克黏 稠性液狀之粗製標題化合物。關於此之急驟層析及分取 之薄層層析U乙酸乙酯·甲醇混合溶劑糸及二氣甲烷· 甲醇混合溶劑糸進行,可得0.5克黏稠性液狀之精製的 標題化合物。 1 Η-Ν MR 光譜(δ ρρπ): 經濟部中央標準局員工消t合作社卬製 (請先閱讀背面之注意事項再填寫本頁) 1.3-1.5(βι,2Η),1.9-2.1(βι,2Η),2.2-3(βι,12Η), 3-3.2(m,2H),3.5-3.8(m,4H),3.8-3.95(in,2H), 6.8- 7 (m,5H),7-7.3(m,8H) 質譜 -22 - 本紙張尺度逍用中國國家標準(CNS)甲4規格(21〇x297&*) 2〇5咖 A6 _B6_ 五、發明説明(21 ) 508 (M + H ) (請先閲讀背面之注意事項再填寫本頁) IR光譜 3400,2800, 1600, 1500, 1150 cm·1 實施例9 1-〔 4,4-雙(4-氣苯基)丁基〕-4-(2-羥基-3-苯硫丙 基)哌阱(化合物9): 5,12克(1 3.3毫莫耳)之1-〔4,4 -雙(4 -氟苯基)丁基〕-4-(2,3 -環氧丙基)哌阱溶解於100毫升乙醇中,於此加入 6.0克(54.5毫莫耳)之苯硫酚,並於室溫下攪拌5小時。 反應混合物注入100毫升之10%氫氧化鈉水溶液中,以 二乙醚萃取後,以無水硫酸鈉乾燥。藉於減壓下蒸除溶 劑,可得5.61克(産率89%)油狀之標題化合物。 NMR (CDC1 a , δ ppm): 1.3-1.5(m,2H),1.9-2.1(m,2H),2.2-2.7(m,12H), 2.9-3.1(m,2H),3.7-3.9(m,2H),6.9-7.4(in,13H), 實施例10 1-〔 4,4-雙(4-氟苯基)丁基〕-4-(2-羥基-3-苯硫丙 基)哌阱♦二鹽酸鹽(化合物10) 經濟部中央標準局员工消費合作杜卬'" 實施例9所得之化合物9之粗體5.61克(11.6毫莫耳) 溶於15毫升乙醇中並加入7.5毫升之4.6H鹽酸-乙醇溶液 ,於室溫下攪拌15分鐘。濾除不溶物後,以二乙醚清洗 2次,藉由再結晶(乙醇)可得5.21克(産率8〗%)白色晶 狀之標題化合物。 本紙張尺度逍用中國Η家橾準(CNS)甲4規格(210x297公釐) A6 B6_ 五、發明説明@2) 熔點:1 7 4 - 1 76 ^ IR (KBr錠劑) 3240,2624-2348,1603,1508,1439,1222,1159,839, 7 6 0cm-1 NMR (DMS〇-d 6 , δ ppm): 1.40-1.60(m,2H),1.99(q,2H,J=8Hz),2.90-3.90 (iB,14H),3.95(t,lH,J = 8Hz),4.12(m,lH),7.00-7. 1 7 ( m, 5H ).7.17-7.40(m.8H) 實施例1 1 1-〔4,4-雙(4-氟苯基)丁基〕-4-(2-甲氧基-3-苯硫 丙基)哌阱(化合物11): 360毫克(0.7毫莫耳)之1-〔4,4-雙(4-氟苯基)丁基〕 -4-(2 -羥基-3-苯硫丙基)哌阱溶解於5毫升之無水四氫 1 經濟部中央標準局員工消費合作杜卬製 (請先閱讀背面之注意事項再填寫本頁) 呋喃中,加入50毫克(1.1毫莫耳)之氫化鈉(純度55%) ,並於室溫下攪拌30分鐘,其次0.12克(0.8毫莫耳)之 甲基碘歴約45分鐘滴下,且更於室溫下攪拌一夜。反應 混合物注入10毫升蒸餾水中,以二乙醚萃取後,以無水 硫酸納乾燥,減壓下,溶劑蒸除後,殘渣以柱層析(矽 膠CHCl3〇CHCl3 :Me0H=100:3)分離。分離之油狀物 溶解於10毫升二乙醚中,並以飽和碩酸鈉水溶液洗淨後 ,以無水硫酸納乾燥。藉由減壓下除去溶劑,可得140 毫克(産率38% )油狀之標題化合物。 本紙張尺度逍用中國國家標準(CNS)甲4規格(210X297公*) Λ 6 B6 五、發明説明(23) HMRCCDC13, δρριη): 1.4- 1.5(m,2H) ,1.9-2.0(m,2H),2.3-2.5(β,12Η), 3.10(d,d,2H,J=7.3Hz,J=17.3Hz),3.18(s,3H), 3.46(t,t,lH,J = 7.3Hz,J = 7.8Hz);6.9-7.0(in,4H), 7.1- 7.2(m,4H),7.2-7.3(m,3H),7,3-7.4(m,2H) 實施例12 1-〔4,4-雙(4-氟苯基)丁基〕-4-(2-甲氣基-3-苯硫 丙基)哌阱♦二鹽酸鹽(化合物12): 實施例1 1所得之化合物1 1之粗體11 0毫克溶解於2毫升 酿中,於此加入1.0毫升之4.6N鹽酸-乙醇溶液,並於室 溫下攪拌30分鐘。濾除不溶物,並以二乙醚清洗2次。 由此所得之粗體藉由再結晶(乙醇:二乙醚= 1:3), 可得80毫克白色晶狀之標題化合物。 I R ( K B r 錠劑): 3 2 4 0 , 2 9 5 0 , 2 4 4 0 , 1 4 8 0 , 1 4 2 0 , 1 2 2 0 , 1 0 9 0 , 8 3 0 cnr1 HMR (DMSO-d 6 , δ ppm ): 1.5- 1.6(m,2H),2.0-2.1(in,2H),3.1-3.8(in,14H), 3.30(s,3H),3.9-4.0(m,lH),4.01(t,lH,J=7.8Hz), 7.1- 7.2(m,4H),7.2-7.4(m,9H) 經濟部屮央標準局貝工消费合作杜,^11 (請先閲讀背面之注意事項再填寫本頁) 訂_ 實施例13 卜(2-乙醯氣基-3-苯硫丙基)-4-〔4,4-雙(4-氟苯基) 丁基〕哌畊(化合物13): 0.49克(1.0毫奠耳)之1-〔4,4-雙(4-氣苯基)丁基〕 本紙張尺度逍用中國國家標準(CNS)甲4規格(210X297公釐) 經濟部中央標準局员工消費合作社.'f製 A 6 _B6_ 五、發明説明) -4-(2-羥基-3-苯硫丙基)哌阱溶解於2毫升Ptt啶中,於 此加入500毫克(5.0毫莫耳)之醋酸酐,並於室溫下攪拌 3.5小時。反應混合物注人15毫升蒸餾水中,以二乙醚 萃取後,以無水硫酸鈉乾燥。減壓下蒸除溶劑後,殘渣 以柱層析(矽膠,CHC134CHC13 :Me0H=100:3)分離。 分離之油狀物溶解於1 0毫升之二乙醚中,以飽和磺酸鈉水 溶液洗淨後,以無水硫酸鈉乾燥。藉由減壓下除去溶劑, 可得410毫克(産率77%)油狀之標題化合物。 N MR (CDC 1 a , δ ppm): 1.3-1.4(m,2H),1.9-2.0(m,2H),1.93(s,3H),2.2-2.3(m,l〇H),2.52(d,2H,J=7.6Hz),3.21(d,d,2H, J = 6.5Hz,J=14.3Hz),3.85(t,lfl,J = 7.3Hz),5.10(ni>lH), 6.8-7.5(m,13H) 實施例14 ,. 1-(2-乙醯氧基-3-苯硫丙基)-4-〔4,4-雙(4-氟苯基) 丁基〕呢阱二鹽酸鹽(化合物14): 實施例13所得之化合物13之粗體410毫克(0.76毫莫耳 )溶解於8毫升醚中,於此加入1.5毫升之4.6N鹽酸-乙醇 溶液,並於室溫下攪拌30分鐘後,濾除不溶物,進一步 再結晶(乙醚:二乙醚= 3:100)此不溶物,可得290毫克 (産率62%)白色晶狀之標題化合物。 IR UBr 錠劑 > : 3350,3000,2350,1740,1510,1220,1040,830 cm'1 NHR (DHS〇-d 6 , δ ppm): 本紙張尺度通用中Η困家標準(CNS)甲4規格(210X297公釐) (請先閱讀背面之注意事項再填寫本頁) 裝· A 6 B6 5〇 五、發明説明(25) 1.6-1.7U,2H).l,99(s,3H),2.1-2.2(m,2H), (請先閱讀背面之注意事項再填窝本頁) 3.2-3.6(m,14H),4.10(t,lH,J=8.1Hz),5.2-5.3 (m,lH),7.1-7.5(m,13H) 參考例1 (S)-(-)-l -〔 4,4-雙(4-氟苯基)丁基〕-4-(2,3-環氧 丙基)呢阱: 經濟部中央標準局員工消費合作社卬製 250毫克(1.1毫莫耳)之(2R) -縮水甘油甲苯磺酸鹽溶 解於3毫升之無水二氣甲烷中,一邊於室溫攪拌,一邊 依序加人含有330毫克(1毫莫耳)1-〔4,4 -雙(4 -氟苯基) 丁基〕哌畊之2毫升無水二氣甲烷溶液,0.4毫升(2.9毫 莫耳)之三乙胺。同溫下拌94小時30分後,將反應液 注入10毫升二氯甲烷,10毫升1H氫氣化鈉水溶液糸中。 分離二氯甲烷層,水層以二氣甲烷萃取(7毫升X2),混 合全部的二氱甲烷層,以飽和食鹽水清洗(10毫升),無水 硫酸鈉乾燥後,蒸除溶劑。殘渣令以矽膠之柱層析(氛 仿,氨仿:甲醇= 100:1),分取氛仿:甲醇= 100:1流 出分劃,並濃縮。殘渣溶解於10毫升之二氣甲烷中,並 以5毫升之1H -氫氧化納水溶液及5毫升飽和食鹽水清洗 ,無水硫酸納乾燥後,蒸除溶劑,可得123毫克(産率 31.9%)油狀之目的物。 IR (KBr 錠劑): 1604,1508,1225,1160,830cm-1 HMR (CDC 1 a , δ ρρβι) 本紙張尺度逍用中Η困家樣準(CNS)甲4規格(210X297公釐) 經濟部中央標準局貝工消費合作社卬製 Λ 6 136 五、發明説明(26) 1.37- 1.50(m,2H),1.99(q,2H,J=8Hz),2.23-2.80 (ra,14H),3.05-3.15(m,lH),3.86(t,lH,J=8HE), 6.90- 7.05(in,4H) ,7.1〇-7.25(m,4H)
Ca]^ -7.4° (c=1.20,CHC13) 參考例2 (R ) -( + )-] -〔4,4 -雙(4 -氟苯基)丁基〕-4-(2,3 -環氣 丙基)哌阱: 使用(2S) -縮水甘油甲苯磺酸鹽同參考例1之方法可 得油狀之目的物。 I R ( K B r 錠劑): 1604,1508,1223,1159,828cm·1 NMR (CDC 1 a , 5 ppm): 1.37- 1.50(in,2H),1.99(q,2H,J = 8Hz),2.23-2.80 » (ra,14H),3.05-3.15(m,lH),3.86(t,lH,J=8Hz), 6.90- 7.05(m,4H),7.10-7.25(m,4H)
Ca]〇0 +7.2C (c=1.28,CHC13) 實施例1 5 (5)-(-)-1-〔4,4-雙(4-氟苯基)丁基〕-4-(2-羥基_ 3-苯硫丙基)哌阱(化合物15)及其二鹽酸鹽(化合物16): 125毫克(0.32毫莫耳)之(S)-(-)-卜〔4,4-雙(4-氟苯 基)丁基〕-4-(2,3-環氧丙基)哌阱溶解於2毫升之乙醇 中,於氬蒙氣下,在室溫一邊攪拌,一邊一次加入5毫升 (0.49毫莫耳)之流苯酚,於同條件下攪拌5小時。其後 本紙張尺度逍用中國國家標準(CNS)甲4規格(210X297公泄) (請先閲讀背面之注意事項再填寫本頁) 裝· 訂- 經濟部中央標準局貝工消費合作社卬製 A 6 Ββ_ 五、發明説明(27) ,反應液注入8毫升乙ffi, 6毫升1H -氫氧化鈉水溶液中 ,分離醚層,水層以醚萃取(6毫升X2)。混合全部的醚 層,以飽和食鹽水(10毫升)清洗,無水硫酸納乾燥後, 蒸除溶劑。殘渣令以矽膠柱層析(氣仿,氯仿:甲醇= 100:1),分取氛仿:甲醇= 100:1流出分劏並濃縮。殘 渣溶解於10毫升醚中,並以5毫升1N氫氧化鈉,5毫升飽 和食鹽水清洗,無水硫酸鈉乾燥後,蒸除溶劑,可得148 毫克(産率91.9%)油狀之目的物(化合物15)。 NMR(CDC13 , d ppm): 1.33-l,48(Bi,2H),1.98(q,2H,J = 8Hz),2.20-2.54 (ra,10H),2.54-2.70(i,2H),2.93-3.10(m,2H), 3.78-3.90(in,2H),6.88-7.02(in,4H),7.05-7.22 (m,5H),7.22-7.33(m,2H),7.33-7.42(m,2H) Ca3 -24.0° (c=1.48,CHC13) 所得之14δ毫克溶解於2毫升醚中,一邊於冰冷下攢拌 ,一邊加入0.1毫升之濃鹽酸。攪拌一陣後,濾取析出 之白色固體,並乾燥,以甲醇-醚(3:1)混合溶劑再結晶 ,可得96毫克(産率56.5%)之目的物之二鹽酸鹽(化合 物 16)。 溶點:1 7 4 - 1 7 6 °C I R ( K B r 錠劑) 3350,2626-2364,1604,1508,1439,1221,1160,838cm-1 NMR(DMS〇-d 6 , δ ppm): (請先閲讀背面之注意事項再填寫本頁) 裝- 訂_ 未紙張尺度逍用中Β國家樣準(CNS)甲4規格(210X297公釐) 經濟部中央標準局貝工消費合作社卬'" A 6 B6 五、發明説明(28) 1.40-1.60(m,2H),1.99(q,2H,J=8Hz),2.90-3.90 (in,14H),3.95(t,lH,J = 8Hz),4.12(in,lH),7.00-7.17 (m,5H),7.17-7.40(in,8H) [a ) %5 -22.3° (c=0.3 ,MeOH) 實施例1 6 (1〇-( + )-1-〔4,4-雙(4-氟苯基)丁基〕-4-(2-羥基-3 -苯硫丙基)呢阱(化合物17)及其二鹽酸鹽(化合物18): 使用(1〇-( + )-1-〔4,4-雙(4-氟苯基)丁基〕-4-(2,3-環氣丙基)哌阱以與實施例15同樣之方法,可得目的物 及目的物之二鹽酸鹽。 化合物1 7 油狀物質 HMR (CDC1 a , δ ppm) 1 1.35-l.50(m,2H),1.99(q,2H,J=8Hz),2.20-2.55 (m,l0H),2.55-2.70(in,2H),2.94-3.l3(Hi,2H), 3.80-3.92(Bi,2H),6.90-7.02 (m,4H),7.l0-7.24 (m,5H ),7.24-7.35(m,2H), (7.35-7.43U,2H) 〔a〕备6 +21.2° (c=1.40,CHC13) 化合物1 8 白色結晶 溶點:1 74 - 1 76 1 I R ( K B r 錠劑): 3350,2626-2364,1603,1507,1439,1220,1160,837cm-1 本紙張尺度逍用中國困家樣準(CNS)甲4規格(210X297公釐) (請先閲讀背面之注意事項再塡寫本頁) 裝- 訂' A 6 Β6 經濟部中央標準局貞工消費合作社卬製 五、發明説明(29) NMR (DMSO-d 6 . δ ppm): 1.40-1.60(m,2H),1.99(q,2H,J=8Hz),2.90-3.90 (a,14H) ,3.95(t,lH,J = 8Hz) ,4.12(m,lH) ,7.00-7.17 (m,5H),7.17-7.40(ffl,8H) [a〕2t7.5 +20.4 0 (c= 0.3 ,MeOH) 實施例1 7 遵從實施例9及10之方法,可得下列化合物。 (1) 1-〔4.4-雙(4-氟苯基)丁基〕-4-C2-羥基-3-(4-甲苯硫基)丙基〕哌阱(化合物19) 油狀物質 NMR (CDC 1 a , δ ρριβ) 1.32-1.48U,2H),l,98(q,2H,J = 8Hz),2.20-2.52 (ra,10H),2.31(s,3H),2.52-2.68(m,2H),2.87-3.06 (ra,2H) ,3.74-3.90(m,2H) ,6.89-7.00(in,4H), 7.03-7.19U,6H),7.23-7.33 (m,2H) (2) 化合物19之二鹽酸鹽(化合物20) 白色結晶 熔點:1 70 - 1 73 1C IR(ICBr 錠劑): 3350,2626-2375,1603,1507, 1450, 1220, 1158,838cm·1 NMR(DMSO-d 6 , δ ppm): 1.55-1.75(m,2H),2.14(q,2H,J=7.5Hz),2.35(s,3H), 3.00-4.00(m,14H),4.10(t,lH,J=7.5Hz),4.22(ra,lH) -3 1- (請先閲讀背面之注意事項再塡寫本頁) 裝- 訂- 線- ‘紙張尺度逍用中國S家樣準(CNS)甲4規格(210X297公釐) Λ 6 Β6 經濟部中央標準局员工消費合作社卬災 五、發明説明(3〇) ,7.10-7.27(m,6H),7.27-7.50(in,6H) (3) 1-〔(4-胺基苯硫基)-2 -羥丙基〕-4-〔4,4 -雙(4-氣苯基)丁基〕哌阱(化合物2 1 ) 油狀物質 NMR (CDC1 3 , δ ppm): 1.33-1.50(m,2H),1.98(q,2H,J=8Hz),2.20-2.52 (m,10H),2.52-2.68(m,2H),2.76-2.95(n,2H), 3.30-3.82(m,3H),3.85(t,lH,J=8Hz),6.55-6.65 (m,2H),6.90-7.03(m,4H),7. 10-7.22(m,4H), 7 . 22-7.32 (m,2H) (4) 化合物21之三鹽酸鹽(化合物22) 白色結晶 溶點:203 -206 ¾ t I R ( O r 錠劑): 3400,266卜2375,1602,1507, 1493,1450, 1413, 1219, 1159,840,820cm-1 NMR (DMS〇-d 6 ,δ ρριβ): 1.57-1.77(m,2H),2.14(q,2H,J=8Hz),2.90-4.05 (m,16H),4.10(t,lH,J=8Hz),4.26(m,lH),7.19 (t,4H,J=9Hz),7.34(d,2H,J=8.5Hz),7.38-7.50 (m,4H),7.56(d,2H,J=8.5Hz) (5) 1-〔雙(4-氟苯基)甲基〕-4-(2-羥基-3-苯甲硫丙 基)哌阱(化合物2 3 ) (請先閲讀背面之注意事項再填寫本頁) 衣紙張尺度遑用中困困家樣準(CNS)甲4規格(210X297公*) Λ 6 Β6 以)3034 五、發明説明(31) 油狀物質 NMR (CDC 1 3 , δ ppm): 2.20-2.47(ni,8H),2.50(q,2H,J = 6Hz),2.53-2.70 (m,2H) ,3.68-3.83(m,lH) ,3.76(s,2H) ,4.20(s,lH), 6.88-7.00(m,4H),7.17-7.40(m,9H) (6) 化合物23之二鹽酸鹽(化合物24) 白色結晶 焰點:1 5 9 - 1 6 2 t I R U B r 錠劑): 3395,3362,2633-2345,1606 ,1513 ,1435,1233 ,116(3, 861,835 cm'1 NMR(DMS〇-d β,δ ppm): 2.80-3.75(m.l0H),3.80(s,2H),4.00-4.60(m,4H), 7.10-7.40(m,9H),7.65-7.95(m,4H) (7) 1-〔3,3-雙(4-氟苯基)丙基〕-4-(2-羥基-3-苯硫丙 基)哌阱(化合物25) 油狀物質 NMR (CDC 1 a , 5 ppm): 2.10-2.28U,4H), 2.28-2.55(m,8H), 2.55-2.80(m,2H), 2.93-3.12(m,2H),3.79-3.91(ni,lH),3.96(t,lH,J = 7Hz), 6.90-7.02(ιβ,4Η),7.10-7.22(πι,5Η)>7.22-7.32(ιβ,2Η), 7.32 -7.42 (m , 2H ) (8) 化合物25之二鹽酸鹽(化合物26) 本紙張尺度通用中B B家標準(CNS)甲4規格(210X297公釐) (請先閲讀背面之注意事項再填寫本頁) 裝- 經濟部中央標準局貝工消費合作社印製 經濟部中央標準局員工消費合作社印製 A 6 Β6 五、發明説明(32) 白色結晶 熔點:1 92 - 1 95 ¾ IR UBr 錠劑): 3282.2622-2402,1603,1580,1509,1439,1231,1160, 827,738 cm'1 NMR (DMSO-d 6 , δ ρρι): 2.80-4.12(m,16H),4.12-4.35(m,2H),7.10-7.33 (ir , 5H) , 7 . 33 -7 . 57 (m , 8H) (9) 1-〔4,4-雙(4-氟苯基)丁基]-4-(2-羥基-3-苯甲硫 丙基)哌阱(化合物27) 油物物質 NMR (CDC 1 a , δ ρριβ): 1.35-1.47(m,2H),1.94-2.03(q,2H),2.26-2.59 f (m,14H),3.71-3.89(m,4H),6.91-7.00(t,t,4H), 7.12-7.34 (m , 9H) (10) 化合物27之二鹽酸鹽(化合物28) 白色結晶 熔點:1 4 5 - 1 4 8 C IR UBr 錠劑): 3400,3000,2600,2500,1500,1200 cm'1 NMRiCDCIa , δ ppm): 1.70-2.85(m,2H),2.08-0.16(q,2H),3.10-3.42 (m,4H),3.60-3.80(m,10H),3.96(t,lH,J=8Hz). 本紙張尺度逍用中B Η家標毕(CNS)甲4規格(210X297公龙) (請先閲讀背面之注意事項再填寫本頁) 裝- 訂_ A 6 B6 五、發明説明(33) 4.10-4.22(m,lH),6.99(t,4H,J=8.9Hz),7.20-7.37 (m,9H) (11) 1-二苯甲基- 4- (2 -羥基-3-苯硫丙基)哌阱(化合物 29) 白色結晶 熔點:1 19-121υ IR (KBr 錠劑): 3800,2800,1600,1500,1180,1100 cnr1 NMR (CDC1 3 , δ ppm): 2.30-2.70(m,10H),2.90-3.20(in,2H),3.30-3.70 (bs,lH),3.80-3.90(m,lH),4.2(s,lH),7.10-7.50 (m,15H ) (12) 1-〔4,4-雙(4-氟苯基)丁基〕-4-〔 3-(4-氣苯硫基 )-2 -羥丙基〕哌阱(化合物30) 油狀物質 HHR (CDC1 a , δ ppm): 1.3-1.5(m,2H),1.9-2.1(q,2H),2,2-2.5(in,10H), 2.5-2.7(m,2H),2.9-3.1(m,2H),3.8-3.9(m,2H), 6.9-7.4(ι,12Η) 經濟部中央標準局貝工消費合作社,-"製 (請先閲讀背面之注意事項再填寫本頁) (13) 化合物30之二鹽酸鹽(化合物31) 白色結晶 熔點:1 6 3 - 1 6 6 1C I R ( K B r 錠劑): 本紙張尺度逍用中Η國家標準(CNS)甲4規格(210X297公釐) 205034 A 6 B6 經濟部中央標準局員工消費合作社印製 五、發明説明(34) 3370.2340.1510.1220.1160.840 era-* N MR (DMSO-d 6 , δ ppm): 1.5- 1.8(m.2H),2‘0-2.3(q,2H),3.0-4.0(m,14H), 4.10(t,lH,J = 7.6Hz),4.2-4.3(in,lH),7.1-7.3 (m,4H),7.4-7.6(m,8H) (14) 1-〔4,4-雙(4-氟苯基)丁基〕-4-〔 3-(3 ,4-二氣苯 硫基)-2 -羥丙基〕哌阱(化合物32) 油狀物質 NMR (CDC1 a , δ ppm): 1.4-1.5(m,2H),1.9-2.1(q,2H),2.2-2.6(in,12H), 2.6- 2.8(m,2fO,3,01(d,2H,J=6.9Hz),3.8-3.9 (m , 2 Η ) , 6 . 9 - 7 . 5 ( m , 1 1 Η ) (15) 化合物2之二鹽酸鹽(化合物33) ,+ 白色結晶 溶點:1 57 - 1 60 1C I R ( K B r 錠劑)·· 3340.2330.1510.1460.1230.1160.840 cm'1 NMR (DMS〇-d 6 , δ ppm): 1.6- 1.8(m,2H),2.1-2.3(q,2H),3.1-4.0(m,14H), 4.10(t,lH,J=7.6Hz),4.2-4.3(ni,lH),7.1-7.8 (m , 1 1 H ) (16) 卜〔4,4-雙(4-氣苯基)丁基〕-4-〔2-羥基- 3-(2-甲氧苯硫基)丙基〕哌阱(化合物34) (請先閲讀背面之注意事項再填寫本頁) 裝· 本紙張尺度逍用中困B家標準(CNS)肀4規格(210X297公*) οro ο
66 AB 五、發明説明(35) 油狀物質 NMR (CDC 1 3 ,5 ppm): 1.3-1.5(m,2H),1.9-2.1(q,2H),2.2-2.7(Hi,12H), 2.9- 3.1(m,2H),3.7-3.9(ffl,5H),6.8-7.4(m,12H) (17) 化合物34之二鹽酸鹽(化合物35) 白色結晶 熔點:1 5 8 - 1 6 1 t I R U B r 錠劑): 3260,2370,1510,1230,1020,830 οπ'1 NMR (DMSO-d 6 , δ ppm): 1.6-1.8(m,2H),2.1-2.2(q,2H),3.0-3.8(m,14H), 3.91(s,3H),4.10(t,lH,J=7.8Hz),4.2-4.3(m,lH), 7.0-7.5(m,12H) (18) 1-〔 4,4 -雙(4 -氟苯基)丁基〕-4-〔 3-(4 -氯苯硫基 )-2-羥丙基〕哌阱(化合物36) 油狀物質 NMR(CDC1b , δ ppm): 1.41(t,t,2H,J=7.8Hz,J=8.1Hz),1.98(d,t,2H, J = 7.8Hz,J = 7.8Hz) ,2.3-2,5(m,10H) ,2.4-2,6(m,2H), 經濟部中央標準局貝工消費合作社卬製 (請先閲讀背面之注意事項再填寫本頁) 2.9- 3.0(m,2H),3.7-3.8(m,lH),3.85(t,lH,J=7.8Hz), 6.9- 7.0(m,6H),7.1-7.2(m,4H),7.3-7.4(in,2H) (19) 化合物36之二鹽酸鹽(化合物37) 白色結晶 本紙張尺度逍用中Η國家標準(CNS)甲4規格(210X297公*) 經濟部屮央標準局員工消費合作社卬製 Λ 6 Β6 五、發明説明(36) 熔點:1 80 - 1 82 ¾ IR UBr 錠劑): 3340,2390,1500,1450,1230,1160,830cm-1 NMR (DMS〇-d 6 , δ ppm): 1.6- 1.7(ra,2H),2.1-2.2(m,2H),3.2-4.0(in,14H), 4.27(t,lH,J=5.9Hz),4.2-4.3(m,lH),7.1-7.6 (m, 1 2H ) (20U-〔4,4-雙(4-氟苯基)丁基〕-4-〔2-羥基- 3-(4-翔苯硫基)丙基〕哌阱(化合物38) 油狀物質 NMR(CDC1 3 , δ ppm): 1.4-1.5(m,2H),2.0-2.1(m,2H),2.3-2.5(m,10H), 2.7- 2.8(m,2H),2.9-3.0(m,2H),3.80(t,lH,J=7.8Hz) f ,3.8-3.9(m,lH),4.9-5.0(br,2H),6.65(d,2H, J=8.4Hz),6.9-7.1(ra,4H),7.1-7.2(m,4H), 7.40(d,2H,J=8.4Hz) (21)化合物38之二鹽酸鹽(化合物39) 白色結晶 焰點:208-210 1: IR (KBr 錠劑): 3250,2390,1510,1270,1160,840 cm'1 NMR (DMS〇-d 6 , δ ρρπι): 1.6-1.7(in,2H),2.1-2.2(ni,2H),3.1-4.0(in>14H), 本紙張尺度逍用中國B家標準(CNS)甲4規格(210X297公*) (請先閲讀背面之注意事項再填寫本頁) >裝- 經濟部中央標準局员工消費合作社.'"製 Λ 6 Β6_ 五、發明説明(37) 4.0- 4.2(m,2H),6.8-6.9(m,2H),7,l-7.2(in,4H), 7.4-7.5(m,6H) (22) 1-〔4, 4-雙(4-氟苯基)丁基〕-4-〔2-羥基- 3-(4-甲氧苯硫基)丙基〕哌阱(化合物40) 油狀物質 NMR (CDC1 a , δ ppm): 1.3- 1.5(m,2H),1.9-2.0(iB,2H),2.4-2.6(B,12H), 2.89(t,2H,J=7.8Hz),3.76(s,3H),3.8-3.9(m,2H), 6.80(dd,2H,J=2.4Hz,J=4.9Hz),6.9-7.0(m,4H), 7.1- 7.2(ni,4H),7.38(dd,2H,J = 2.4Hz,J = 4.9Hz) (23) 化合物40之二鹽酸鹽(化合物41) 白色結晶 熔點:1 82 - 1 85 ¾ I R ( K B r 錠劑): 3350,2940,2380,1600,1440,1220,830 cm'1 NMR (DMS〇-d 6 , δ ρρm): 1.4- 1.6(i,2H),2.0-2.2(m,2H),2.3-2.7(m,12H), 2.9-3.0(m,2H),3.83(s,3H),3.9-4.0(m,2H), 6 . 8-7 . 2 (in, 12H) (24) 1-〔4, 4 -雙(4 -氣苯基)丁基〕-4-〔2 -羥基- 3- (3-甲氧苯硫基)丙基〕哌阱(化合物42) 油狀物質 NMR (CDC1 a , 5 ppm): (請先閲讀背面之注意事項再填寫本頁) 裝- 訂_ 本紙張尺度逍用中國因家標準(CNS)甲4規格(210x297公*) A 6 B 6 經濟部中央標準局員工消費合作社印製 五、發明説明(38) 1.4- 1.5(m,2H),1.9-2.0(m,2H),2.3-2.5(m,10H), 2.6-2.7(ih,2H),2.9-3.0(i,2H),3.76(s,3H),3.8-3.9 (m,2H),6.6-6.7(ni,lH),6.9-7.0(in.6H),7.1-7.2 (m,5H ) (25) 化合物42之二鹽酸鹽(化合物43) 白色結晶 熔點:1 75 - 1 78 C I R U B r 錠劑): 3250,2920,2430,1600,1470,1290,1160,1040,840cm·1 NMR (DMS〇-d e , δ ppm): 1.5- 1.7(ni,2H),2.0-2.2(ra,2H)’2.3-2.8(m,12H), 3.0-3.2(hi,2H),3.80(s,3H),3.9-4.0(ih,2H),6.9-7.0 (ιπ,5Η),7.1-7.3(πι,4Η),7.4-7.5(ιη,3Η) (26) 卜〔雙(4-氟苯基)甲基〕-4-〔2-羥基- 3-(2-甲氣苯硫基)丙基]哌阱(化合物44) 油狀物質 NMR (CDC1 3 , 5 ppm): 2.4-2.6(in,12H),2.9-3.1(nt,2H),3.8-3.9(in,lH), 3.87(s,3H),4.19(s,lH),6.8-7.0(in,6H),7.1-7.4 (m , 6 Η ) (27) 化合物44之二鹽酸鹽(化合物45) 白色結晶 焰點:1 6 0 - 1 6 3 t -40 - (請先閱讀背面之注意事項再填寫本頁) 裝- 訂_ 本紙張尺度逍用中國困家標準(CNS)甲4規格(210x297公釐) 經濟部中央標準局员工消費合作社卬製 ‘一〇3价! 五、發明説明(39) I R ( K B r 錠劑): 3250,2300,1580,1510,1440,1280,840 cm'1 NMR(DMS〇-d 6 , δ p p m): 3.1- 3.3(bi,4H),3.5-3.7(hi,9H),3.65(s,3H), 4.15(t,lH,J=7.3Hz),8.90(d,2H,J=8.9Hz), 7.2- 7.3(iB,4H),7.42(d,2H,J = 8.9Hz),7.8-8.0 (m,4H ) (29) 1-(2,2-二苯乙基基)-4-(2-羥基-3-苯硫丙基)哌阱 (化合物4 6 ) 油狀物質 NMR (CDC1 a , 5 ppm): 2.3- 2.6(®,10H),2.9-3.1(m,4H),3.7-3.9(in,lH), 4,18(t,lH,J=7.6Hz),7.1-7.4(m,15H) (30) 化合物46之二鹽酸鹽(化合物47) 白色結晶 馆點:163 - 1 65 = IR (KBr 錠劑): 3430,2360,1450,1090,740 cm'1 NMR (DMS〇-d 6 , δ ρ ρ πι): 3.2-3.7(m,12H),4.0-4.2(m,2H),4.27(t,lH, J=6.8Hz),4,80(brs,lH),7.2-7.6(m,15H) (31) 1-(3,3-二苯丙基 )-4-(2-羥基-3-苯硫丙基)哌阱 (化合物4 8 ) A 6 B6 (請先閲讀背面之注意事項再填寫本頁) 本紙張尺度逍用中B國家標準(CNS)甲4規格(210X297公釐) 經濟部中央標準局貝工消費合作社印'" A 6 B6_ 五、發明説明(40) 油狀物質 NMR (CDC 1 a , δ ρρπι): 2.2-2.7(βι,14Η),2.9-3.1(πι,2Η),3.8-3.9(βι,1Η), 3.97(t,lH,J=6.8Hz),7.1-7.4(m,15H) (32) 化合物48之二鹽酸鹽(化合物49) 白色結晶 熔點:1 93 - 1 96 ¾ IR UBr·錠劑): 3270,2990,2350,1490,1090,740 cm·1 NMR (DMSO-d 6 , δ ρρπι): 2.5-2.7(in,2H),3.1-3.9(m,16H),4.14(t,lH, J=7.3Hz),4.2-4.3(m,lH),7.2-7.5(m,15H) (33) 1-(4,4-二苯丁基 )- 4-(2-羥基-3-苯硫丙基)哌哄 t (化合物5 0 ) 油狀物質 NMR (CDC1 3 , δ ppm): 1.36(t,t,2H,J=7.6Hz,J=7.8Hz),1.95(d,t,2H, J = 7.8Hz,J = 7.8Hz),2.1-2.7(in,12H),2.9-3.0 (i»,2H),3.7-3.8(in,2H),7.0-7.3(iii115H) (34) 化合物50之二鹽酸鹽(化合物51) 白色結晶 熔點:1 9 7 - 1 9 9 I R ( K B r 錠劑): (請先閲讀背面之注意事項再填寫本頁) -裝- 訂- 本紙張尺度逍用中困國家標準(CNS〉甲4規格(210X297公釐) hο ΰο
66 AB 經濟部屮央標準局貝工消費合作社卬奴 五、發明説明(41) 3220,2500,1 470,1240,1070,760 cm-1 NMR (DMSO-d 6 , δ p p in): 1.6- 1.7(m,2H),2.1-2.2(i,2H),3.2-3.9(m,14H), 4.05(t,lH,J=6.8Hz),4.2-4.3(ni)lH))7.2-7.5 (m, 15H) (35U-〔雙(4-氟苯基)甲基〕-4-(2-羥基-3-苯硫丙基) 呢阱(化合物5 2 ) 油狀物質 NMR (CDC 1 a , δ ppm): 2.3-2.5(m,8H),2.5-2.6(m,2H),2.9-3.1(m,2H), 3.8-3.9(m,lH),4,19(s.lH),6.9-7.0(m,4H), 7.1-7.4(π,9Η) (3 6 )化合物5 2之二鹽酸鹽(化合物5 3 ) 白色結晶 焰點:1 43 - 1 46 C IR (KBr 錠劑): 3480,2430,1610,1500,1440,1240,830 cm'1 NMR(DMS〇-d 6 , δ ppm): 2.7- 3.2(m,4H),3.4-3.7(m,9H),4.16(t,lH,J=4.1Hz) ,7.2-7.4(m,10H),7.6-7.7(io,3H) (37)1-〔雙(4-氣苯基)甲基〕-4-〔2-羥基- 3-(4 -甲氣 苯硫基)丙基)哌畊(化合物54) 油狀物質 (請先閱讀背面之注意事項再填寫本頁) 本紙張尺度逍用中困國家標準(CNS)甲4規格(210x297公釐) Λ 6 B6 經濟部屮央標準局員工消費合作社.^111 五、發明説明(42) NMR (CDC1 a , 5 ppm): 2.4-2.6(m,10H),2.9-3.0(m,2H),3.6-3.7(ni,lH), 3.69(s,3H),4.20(s,lH),6.8-7.0U,6H),7.3-7.4 (m , 6H ) (38) 化合物54之二鹽酸鹽(化合物55) 白色結晶 熔點:1 62 - 1 64 Ό IR (KBr 錠劑): 3260,2300,1610,1490,1440,1280,830 cm·1 NHR(DMS〇-d e , δ ppra): 3.0- 3.2(m,2H),3.4-4.0(m,llH).3.78(s,3H), 4.0- 4.1(B,lH),6.89(d,2H,J=8.9Hz),7.22(t, 4H,J=8.4Hz),7.39(d,2H,J=8.9Hz),7.7-7.8 1 (m,4H) (39) 1-〔4,4-雙(4-氟苯基)丁基]-4-〔2-羥基- 3-(1-萘硫基)丙基〕哌阱(化合物56) 油狀物質 NHR (CDC1 a , δ ppm): 1.2-1.4U,2H),2.0-2.1(m,2H),2.3-2.6(m,18H), 3.0- 3.1(m,2H),3.84(t,lH,J=7.0Hz),6.9-7.0 (πι,4Η),7.1-7.2(πι,4Η),7.4-7.9(ιβ,6Η),8.43 (d,1H,J = 8. 1Hz) (40) 化合物56之二鹽酸鹽(化合物57) -44- (請先閲讀背面之注意事項再填寫本頁) 裝· 本紙張尺度逍用中國困家標準(CNS)甲4規格(210父297公釐) Λ 6 Β6 經濟部中央標準局員工消費合作社卬製 五、發明説明(43) 白色結晶 熔點:1 8 0 - 1 8 2 υ IR (Or 錠劑): 3 3 00,2240,1510,1470,1200,830 cm'1 HMR (DMS〇-d 6 , δ ppm): 1.6-1.7(ιπ,2Η),2.1-2.2(ιη,2Η),3.2-3.9(ιη,1δΗ), 4.10(t,lH,J=7.3Hz),4.3-4.4(ra,lH),7.2-7.7 (ra,llH),7.78(d,lH,J=7.6Hz),7.92(d,lH,J=7.6Hz) ,8.04(d,lH,J=7.6Hz),8.36(d,lH,J=7.6Hz) (41) 1-〔 4,4-雙(4-氟苯基)丁基〕-4-(2-羥基- 3-(N-甲 基-N-苯胺基)丙基〕哌阱(化合物58) 油狀物質 NMR(CDC]a , δ ppm): 1.35-1.52(a,2H).1.99(q,2H,J = 8Hz).2.25-2.56 (ra,10H),2.56-2.76(Hi,2H),2.99(s,3H),3.37 (d,2H,J=9.5Hz).3.86(t,lH,J=8Hz),3.91-4.05 (m,lH) ,6.68-6.83(m,3H) ,6.92-7.07(id,4H), 7.10-7.33(m,6H) (42) 化合物58之三鹽酸鹽(化合物59) 白色結晶 擦.點:1 92 - 1 95 ¾ I R U B r 錠劑): 3425,3235(shoulder),2638-2450,1603,1509, -4 5 _ (請先閱讀背面之注意事項再填寫本頁) 裝- ,1T_ 本紙張尺度逍用中困S家標毕(CNS)甲4規格(210X297公*) A 6 B6 五、發明説明(44) 1222,1158,835 cm'1 NMR (DMS〇-d 6 , δ p p in): 1.56-1.76(in,2H),2.04-2.20(in,2H),3.06(s,3H), 3.12-3.98(m,14H),4.10(t,lH,J=8Hz),4.16-4.42 (ra,lH),6.83(t,lH,J=7.3Hz),6.98(d,2H,J=7.3Hz), 7.19(t,4H,J=8.6Hz),7.30(t,2H,J=7.7Hz),7.35-7 . 50 (m , 4H ) (43U -〔4, 4 -雙(4 -氟苯基)丁基〕-4-〔 3-(3,4 -二甲氧 苯硫基)-2 -羥丙基〕哌阱(化合物60) 油狀物質 NMR(CDC13 , δ ppm): l,3-1.4U,2H),1.9-2.0(m,2H),2.3-2.7(m,12H), 3.8-4.0(in,2H),3.84(s,3H),3.85(s,3H),6.9-7.0 (m , 7H) , 7 . 1 -7 . 2 (in , 4H) (44)化合物60之二鹽酸鹽(化合物61) 白色結晶 熔點:139-141υ I R ( K B r 錠劑): 經濟部屮央標準局員工消費合作社印製 (請先閱讀背面之注意事項再填寫本頁) 34 3 0,2950,2360,1450,1020,830 cm'1 NMR (DMSO-d 6 , δ ρριπ): 1.5-1.6(®,2H),2,0-2.1(m,2H),3.1-3.7(m,14H), 3.74(s,3H),3.77(s,3H),4.0-4.1(in,lH),4.01 (t,lH,J = 8Hz) ,6.9-7.1 (m,6H) ,7.3-7.4(m,5H) -46 -本紙張尺度逍用中B國家標毕(CNS)甲4規格(210X297公*) IV- 3^o 5o
66 AB 經濟部屮央標準局貝工消費合作社印览 五、發明説明(45) (45) 1-〔 4,4-雙(4-氣苯基)丁基〕-4-〔 3-(4-氨苯甲硫 基)-2 -羥丙基〕哌阱(化合物62) 油狀物質 NMR (CDC 1 a , 5 ppm): 1.4- 1.5(m,2H),2.0-2.1(m,2H),2.3-2.5(m’12H), 2.6-2.7(m,2H),3.7-3.8(m,3H),3.86(t,lH,J=8.1Hz) ,6.9-7.0(m,4H),7.1-7.2(m,4H),7.2-7.3(in,4H) (46) 化合物62之二鹽酸鹽(化合物63) 白色結晶 熔點:1 3 6 - 1 38 1 IR(KBr 錠劑) 3320,2550,2340,1450,1160,1090,840cm·1 NMR (DMS〇-d 6 , 8 ppm): 1.5- 1.6(in,2H),1.9-2.0(in,2H),3.Q-3.8(in,14H), 3.74(s,2H),3.95(t,lH,J=8.1Hz),4.1-4.2(m,lH), 7 . 0-7 . 1 (m , 4H) , 7 . 2-7.3 (a,8H), (47) 1-〔4,4-雙(4-氟苯基)丁基〕-4-〔2-羥基- 3-(4-甲氧苯甲硫基)丙基〕哌阱(化合物64) 油狀物質 HMR (CDC1 3 , d ppm): 1.5- 1.6(in,2H),2.0-2.1(in,2H),2.4-2.7(in,14H), 3.81(s,2H),3.84(s,3H),3.8-3.9(m,lH)>3.96 (t,lH,J = 8.1Hz),6.9-7.0(m,2H),7.0-7.1(ni,4H), 本紙張尺度逍用中國國家標準(CNS)甲4規格(210x297公釐) (請先閲讀背面之注意事項再填寫本頁) 裝· 訂. Λ 6 Β6 五、發明説明(46) 7.2-7.3(m,4H),7.4-7.5(m,2H) (48) 化合物64之二鹽酸鹽(化合物65) 白色結晶 熔點:1 62 - 1 6 4 1C I R ( K B r 錠劑): 3320,2870,2 3 60,1450,1250,840 cm'1 HMR (DMS〇-d 6 , δ ppm): 1.5-1.6(m,2H),2.0-2.1(ni2H),3.1-3.8(ra,14H), 3.72(s,3H),3.75(s,2H),4.04(t,lH,J=8.1Hz), 4.1- 4.2(n,lH),6.89(d,2H,J=8.9Hz),7.1-7.2 (m,4H) ,7,26(d,2H,J = 8.9Hz) ,7.3-7.4(m,4H) (49) 卜〔4,4-雙(4-氣苯基)丁基]-4-〔2-羥基-3-(3-苯丙硫基)丙基〕哌阱(化合物66) 油狀物質 NMR(CDCla , δ ppm): 1.4-1.5(m,2H),1.9-2.1(m,4H),2.3-2,7(m,18H),3.7 -3.8(iB,lH),3.85(t,lH,J = 8.1Hz),6.9-7.0(m,3H), 7.2- 7.3(m,10H) (50) 化合物66之二鹽酸鹽(化合物67) 經濟部中央標準局員工消費合作社卬製 (請先閲讀背面之注意事項再填寫本頁) 白色結晶 熔點:1 83 - 1 86 ¾ I R ( K B r 錠劑): 3430,2340,1650,1510,1160 cm'1 一 4 8 _ 本紙張尺度逍用中國困家標準(CNS)甲4規格(210x297公釐) 經濟部中央標準局員工消費合作社卬製 A 6 Β6 五、發明説明(47) NMR (DMS〇-d 6 ,8 ppm): 1.6- 1.7(i,2H),1.92(Sep,2H,J=7.6Hz),2.1-2.2 (m,2H), 2.6-2.8(m,8H),3.1-3.8(m,10H),4.10 (t,lH,J = 7.6Hz),4.2-4.3(m,lH),7.2-7.5(ni,13H) (51Π -〔4,4 -雙(4 -氟苯基)丁基〕-4-〔2 -羥基-3-(4-硝苯硫基)丙基〕哌阱(化合物68) 油狀物質 NMR (CDC1 a , δ ppm): 1.3- 1.5(m,2H),1.9-2.1(q,2H),2.2-2.7(in,12H), 3.1- 3.2(d,2H),3.86(t,lH,J = 7.7Hz),3.9-4.0(ni>lH) ,6.9-7.0(ni,4H),7.1-7.2(m,4H),7.4-7.5(ni,2H), 8.1- 8.2(in,2H) (52)化合物68之二鹽酸鹽(化合物69) t 淡黃色結晶 熔點:1 84 - 1 87 1C IR (KBr 錠劑): 3420,2360,1510,1340,1220,1090, 84 0 cm·1 NMR (DMS〇-d 6 , δ ρρm): 1.6- 1.8(ΐΒ,2Η),2.1-2.3(ς,2Η),3.1-3.9(ιι,14Η), 4.10(t,lH,J=8.1Hz),4.2-4.4(ra,lH),7.1-7.3(m,4H), 7.3- 7.5(m,4H),7.6-7.7(m,2H),8.2-8.3(m,2H) 參考例 3 N-(2,3 -環氧丙基)-N -甲磺醯苯胺之合成 -49- 本紙張尺度逍用中國B家標準(CNS)甲4規格(210X297公釐) (請先閱讀背面之注意事項再填寫本頁) 裝. 訂_ Λ 6 Β6 五、發明説明(48) 1.7克之Ν -甲磺醯苯胺(0.0〗莫耳)溶解於]〇〇毫升之二 氣甲烷中,並加入7克(0.051莫耳)之表溴醇。於此徐 徐加入溶有12克溴化四甲基銨(0.047莫耳)和2克氫氧化 鈉(0.05莫耳)之5毫升水。攪拌一夜。以50毫升水清洗3 次後蒸除二氛甲烷。此以矽膠層析精製,可得1.9克(産 率8 3.7% )之淡黃色油狀標題化合物。 IR (KBr 錠劑): 1595,1499,1337,1 160 cm'1 NMR (CDC 1 a , 5 ppm): 7.27-7.47(m,5H),3.72-4.13(m,2H),3.15-3.21 (πι,ΙΗ) ,2.97rs,3H) ,2.76-2.80(dd,lH) ,2.52-2.54 (dd , 1 H ) 實施例1 8 卜〔4,4-雙(4-氟苯基)丁基〕-4-〔2-羥基- 3-(N -甲 礎醯基-N-苯胺基)丙基〕哌畊(化合物70)及其二鹽酸鹽 (化合物7 1 ) 經濟部屮央標準局員工消費合作社.---11製 (請先閲讀背面之注意事項再填寫本頁) 1.9克之N-(2,3-環氧丙基)-N -甲磺醯苯胺(0.083莫 耳)與3.3克(0,01莫耳)1-〔 4,4-雙(4-氟苯基)丁基〕哌 阱溶解於100毫升乙醇中,並在室溫攪拌一夜。由此反 應物蒸除溶劑後,殘渣以矽膠層析精製,可得2.8克(産 率62% )之淡黃色油狀目的化合物(化合物70)。 其中之1克溶解於無水酒精中,並滴下2毫升濃鹽酸 後蒸除溶劑,可得1.12克(産率98.6%)白色無定形之目 -50 -本紙張尺度逍用中國國家標準(CNS)甲4規格(210X297公龙) ί^050〇4 Λ 6 Β6 經濟部屮央標準局貝工消費合作社印'" 五、發明説明(49 的化合物的二鹽酸鹽(化合物71)。 化合物70 HMRCCDCls ,(5ppm): 7.65-'7.31(βι,5Η),7.17-7.11(ιιι,4Η),7.02-6.87(βι,4Η) ,3.88-3.70(m,3H),3.65-3.48(m,lH),3.01(s,3H), 2.47-2.27(m,12H),2.09-1.93(2H),1.52-1.23(m,2H) 化合物7 1 I R ( K B r 錠劑): 2649.2558,2438,1602,1508,1334,1222,1156 cm'1 NMR(CD3 0D,5 ppm): 7.87-7.27(m,9H),7.04-7.27(ni,4H),4.24-3.31 (Hi,16H),2.97(s,3H),2.15-2.02(ra,2H), 1.73(bs,2H) t 參考例4 N-(2,3-環氧丙基)-N-(4 -甲苯基)磺醯苯胺之合成 於0·48克(12.0毫莫耳)氫化納(60%)之無水DMF 10毫 升懸濁液中,氬蒙氣下,一邊於室溫下攪拌,歴10分鐘 滴下加有2.59克(10.5毫莫耳)Ν-(4-甲苯基)磺醯苯胺之 10毫升無水DMF溶液,並於同條件下攪拌30分鐘。於此 同條件下,歴10分鐘滴下加有1.37克(10.0毫莫耳)表溴醇 之10毫升無水DMF溶液,並繼績於同條件下攪拌22小時。 其後,反應液注入2 0 0毫升冰冷之0 . 5 Ν -氫氧化納中,以 醚萃取(50毫升X 3)。混合全部醚層以水(50毫升X 3), -5 1 - (請先閲讀背面之注意事項再填寫本頁) 裝· 本紙張尺度逍用中國國家標毕(CNS)甲4規格(210X297公釐) 經濟部中央標準局貝工消费合作社卬製 *ό〇5〇〇^ Λ 6 _Β6_ 五、發明説明(5〇) 飽和食鹽水(50毫升)清洗,無水硫酸鈉乾燥後,蒸除溶 劑。殘渣油狀物質以正-已烷以潷析法清洗3次,藉由滅 壓乾燥,可得2.00克(産率66.0%)黃色固體目的物。 熔點:7 5 - 7 8 I R ( K B r 錠劑): 1594,1493,1343.1164,1093,1065,863 ci'1 HMR (CDC 1 a , δ ppm): 2.36-2.48(m,lH),2.39(s,3H),2.67-2.73(ra,lH), 3.08-3.18(ιπ,1Η),3.58-3.77(ιβ)2Η),7.03-7.13 (m,2H),7.20-7,36(m,5H),7.44-7.54(m,2H) 實施例1 9 1-〔4, 4-雙(4-氟苯基)丁基〕-4-〔2-羥基-3- {N-(4 -甲苯基)磺醯基-N-苯胺基)丙基〕哌胼(化合物72)及 其二鹽酸鹽(化合物73) 使用參考例所得之原料,同實施例1 8處理可得標題化 合物。 化合物7 2 油狀物質 NMR (CDC 1 a , δ ppjh): 1.31-1.46(m,2H),1.98(q,2H,J=8Hz),2.20-2.39 (ra,8H),2.41(s,3H),2.46-2.60(in,4H)>3.59(d,2H, J=6Hz),3.64-3.77(in,lH),3.85(t,lH,J = 8Hz),6.95 (tt,3H,J = 2.5,9Hz),7.01-7.09(ni,2H),7.09-7.19 (請先閱讀背面之注意事項再填寫本頁) 本紙張尺度逍用中國國家標準(CNS)甲4規格(210X297公釐) ςΰο 5ο 66 ΛΒ 經濟部中央標準局貝工消費合作杜卬製 五、發明説明(51) (m,4H),7.19-7.33(m,6H),7.45(d,2H,J=8.5Hz) 化合物73 白色結晶 熔點:132-136Ό IR (KBr 錠劑): 3440,3330,3299,2643-2437,1625 (shoulder),1601, 1508,1454,1335,1223,1161,835,823 cm·1 NMR (DMS〇-d 6,δ ρρπι): 1.55- 1.77(m,2H),2.05-2.2(m,2H) ,2.49(s,3H) ,3,00 ) -3.95(m,14H),3.95-4.05(m,lH),4.11(t,lH,J=8Hz), 7.10-7.27(n,6H),7.27-7.57(m,llH) 實施例20 同實施例1 8處理可得下列化合物。 (1) l-〔3-U-乙醯基-N-苯胺基)-2-羥丙基〕-4_〔4,4 -雙(4 -氟苯基)丁基〕哌阱(化合物74) 油狀物質 NMR (CDC 1 a , δ ρριπ): 1.31-1.47(m,2H),1.86(s,3H),l.90-2.05(m,2H), 2.20-2.47(m,10H),2.47-2.63(nt,2H)>3.60-4.00 (ra,4H),6.88-7.00(in(4H),7.07-7.20(in,4H),7.20 -7.28(ffl,2H),7.28-7.46(m,3H) (2) 化合物74之二鹽酸鹽(化合物75> 白色結晶 (請先閲讀背面之注意事項再填寫本頁) 裝· 訂- 線. 本紙張尺度逍用中國國家樣準(CNS)甲4規格(210乂297公龙) Λ 6 136 經濟部中央標準局貝工消f合作社印11 五、發明説明(52) 熔點:182-185Ό I R ( K B r 錠劑): 3400,3275(shoulder),2650-2464, 1651,1594,1508, 1223,833 cm'1 NMR (DMS〇-d 6 , δ ppm): 1.53-1.74(m,2H),1.80(s,3H),2.00-2.22(m,2H), 3.00-4.05(ra,14H),4.11(t,lH,J=8Hz),4.16-4.30 (ra,lH),7.20(t,4H,J=9Hz),7.30-7.50(m,5H), 7.50 -7.63 (m , 4H ) (3) 1-〔4,4-雙(4-氟苯基)丁基〕-4-〔3-(1<,1<-二苯胺 基-2 -羥丙基〕哌阱(化合物76) 油狀物質 N MR (CDC 1 a , δ ρρπι): 1.30-1.45(πι,2Η),1.90-2.10(q,2H),2.20-2.45(ιη, 10H),2.45-2.60(m,2H),3.70-3.75(m,2H),3.83 (t,lH),3.95-4.10(ra,lH),6.90-7.00(ni16H),7.05 (d, 4H), 7.05-7.15 (m, 4H;, 7.20 (t, 4H). (4) 化合物76之二鹽酸鹽(化合物77) 白色結晶 熔點:104-1 12*C I R ( K B r 錠劑): 3330,2923,2560,2366,1595,1502,1450,1225,1159, 832,755,699 cm—1 -54- (請先閲讀背面之注意事項再填寫本頁) 裝· 訂- 線· 本紙張尺度逍用中Η Η家標準(CNS)甲4規格(210x297公煃) Λ 6 136 五、發明説明(S3) NMR (DMSO~d e , δ ppm): (請先閱讀背面之注意事項再填寫本頁) 1.60-1.70(m,2H) ,1.90-2. 20(q,2H) ,3.00-3.90(m, 14H),4.03(t,lH),4.20-4.30(m,lH),6.90-7.00 (t,2H),7.00-7.15(ni,8H),7.20-7.40(in,8H) (5) 1-〔4,4-雙(4-氟苯基)丁基〕-4-〔2-羥基- 3-(N-苯 基-N-苯甲胺基)丙基〕哌阱(化合物78) 油狀物質 NMR (CDC1 a , δ ppm): 1.30-1.50(m,2H),1.90-2.05(q,2H),2.20-2.50 (ra,10H),2.50-2.70(Ht,2H),3.47(d,2H),3.85(t,lH), 4.00-4.10(m,lH),4.66(d,2H),6.65-6.80(ffl,3H), 6.90-7.00(m,4H),7.00-7.30(m,llH) (6) 化合物78之三鹽酸鹽(化合物79) 白色結晶 熔點:112-118C IR (KBr 錠劑): 3554,3411,2565,1602,1506,1225,832 cm'1 NMR (DMSO-d β , δ ρριβ): 1.50-1.70(m,2H) ,2.00-2. 15(ιη,2Η) ,3.00-3.90 經濟部屮央標準局貝工消费合作社.''f製 U,14H),4.03(t,lH),4.40-4.50(m,lH),4.67(s,2H), 6.62(t,lH),6.79(d,2H),7.0〇-7.40(in,15H) (7) 1-〔4,4-雙(4-氟苯基)丁基〕-4-〔3-(^-乙氧羰基-N -苯胺基)-2 -羥丙基〕哌阱(化合物80) -55-各紙張尺度逍用中國困家標準(CNS)甲4規格(210><297公龙) 3o rjo ία 66 ΛΒ 經濟部中央標準局貝工消费合作杜..^-¾. 五、發明説明(54) 油狀物質 NMR (CDC1 3 , 5 ppm): 1.1- 1.3(t,3H,J = 6.9Hz),l.3-1.5(ai,2H),1.9-2.1 (q,2H),2.2-2.7(Hi,14H),3.5-4.0(m,2H),4.14(q, 2H , J = 6 . 9Hz),6.9-7 - 5 (m, 13H) (8)化合物80之二鹽酸鹽(化合物81) 白色結晶 I R ( K B r 錠劑): 3420,2560,1510,1220,1160,830cm·1 NHR (DMS〇-d 6 ,δ ρριβ): 1.1- 1.3(t,3H,H=6.9Hz),1.6-1.8(m,2H),2.1-2.2 (q,2H,J=7.6Hz),2.9-3.9(ni,14H),4.1-4.3(in,4H), 7.1- 7.5(m,13H) 實施例21 同實施例11及1 2處理可得下列化合物。 (1)1-〔4,4-雙(4-氟苯基)丁基〕-4- [2-苯醯氣基- 3-苯硫丙基〕哌阱(化合物82) 油狀物質 NMR (CDC1 3 , δ ppm): 1.4-1.5(ιη,2Η),1.9-2.0(ιη,2Η),2.3-2.6(ιη,12Η)> 3.6-3.7(B,lH),3.86(t,lH,J=7.8Hz),4.59(d,2H, J=3.0Hz),6.9-7.0(m,4H),7.1-7.2(in,5H),7.2-7.4 (m,9H) -56 二 (請先閱讀背面之注意事項再填寫本頁) 本紙張尺度逍用中國國家標準(CNS)甲4規格(210X297公龙) Λ 6 Β6 經濟部中央標準局貝工消t合作杜.#11 五、發明説明Ρ5) (2) 化合物82之二鹽酸鹽(化合物83) 白色結晶 熔點:84- 86它 I R ( K B r 錠劑): 3440,2930,2550,2450,1510,1220,1060,840cm-1 NMR (DMS〇-d e , δ ppm) · 1.6-1.7(m,2H),2.1-2.2(m,2H),3.2-3.8(n,14H), 4.0- 4.1(m,lH),4.3-4.4(in,lH),4.6-4.4(s,2H), 7.1- 7.2(m,4H),7.4-7.6(m,14H) (3) 1-〔4,4-雙(4-氟苯基)丁基〕-4-〔2-乙氣羰基甲氧 基-3 -苯硫丙基〕哌阱(化合物84) 油狀物質 I R ( K B r 錠劑): 1 3410,2940,1740,1510,1280,1160,830cm-1 NMR (CDC1 3 , δ ppm): 1.28(t,3H,J = 7.6Hz),1.3-1.5(m,2H),1.9-2.0(in,2H) ,2,3-2.7(m,12H),3,l-3.2U,2H),3.63(t,lH,J=5.9 Hz),3.85(t,lH,J=7.8Hz),4.17(q,2H,J=7.6Hz), 4.24(s,2H),6.9-7.0(m,3H),7.1-7.2(m,4H),7.2-7.3 (m,2H),7.3-7.5(m,4H) 實施例22 1-苯硫甲基-2-〔4- {4,4 -雙(4 -氟苯基)丁基}哌畊 乙氣醋酸鈉(化合物8 5 ) (請先閲讀背面之注意事項再填寫本頁) 裝. 訂- 線. 表紙張尺度逍用中國國家標準(CNS)甲4規格(210x297公愛) Λ 6 Β 6 經濟部中央標準局貝工消費合作杜.'f製 五、發明説明(56) 0.05克(0.88毫莫耳)1-〔4,4 -雙(4 -氟苯基)丁基〕-4 -〔2 -乙氣羰基甲氧基-3-苯硫丙基〕哌阱溶解於10毫升 甲醇中,並加入1.75毫升之2.ON NaOH水溶液,並於氬 氣下取代後,在室溫攪拌2小時。反應液注入50毫升蒸 餾水中,以稀鹽酸還原為中性後,以苯萃取。 無水硫酸鈉乾燥後,減壓蒸除溶劑,並將殘留物以柱 層析(矽膠,CHC13 :MeOH=97:3)分離。生成物更以20 毫升苯溶解,以飽和磺酸鈉清洗後,藉由乾燥,蒸除溶 劑,可得220毫克(産率46%)之油狀標題化合物。 NMR(CDCI3 , δ ppm): 1.3-1.4(m,2H)’1.9-2.0(m,2H),2.40(t,J=7.6Hz,2H) ,2.6-3.1(m,12H),3.6-3.7(m,lH),3.84(t,lH, J=7.8Hz),4.07(ABq,2H,J=17.3Hz),6.9-7.0(ra,4H), 7.1-7.2(m,4H),7.2-7.3(m,5H) 試驗例1 鈣拮抗作用: 本發明之二苯基哌阱衍生物及氟苯桂阱之鈣拮抗作用 試驗以下列方法進行。 W i s t a r株公鼠(3 0 0〜3 5 0克)令以放血致死,於開胸下 摘出胸部大動脈,並做成約3〜4毫米之環標本。標本懸 垂於通以混合氣體(95% 02, 5%C〇2)充滿37±0.5*C Krebs Henseleit之Magnas管中。令以約2克之負荷並記 錄張力變化的等尺性。 鈣拮抗作用所示為抑制KC1濃度依賴收縮(10〜6〇mM) 之最大收縮5 0 %之供試藥物濃度(Μ )。結果示於表]。 (請先閱讀背面之注意事項再填寫本頁) 裝- 線- 本紙張尺度通用中國國家標準(CNS)甲4規格(210X297公釐) 五、#明說明(57) Α6 Β6 經濟部中央標準局員工消費合作社卬製 化合物Wo. 5 0 %抑制狻度(M) 3 1.3X10-8 4 1.3X10'6 5 1. 2X10-6 6 2. 2X10-1 1 0 1.6X10"7 12 2.0X10'1 14 2.8X10-7 16 1. ΟΧΙΟ'1 18 i.axi〇"7 2 0 2.7X10-7 2 2 6.3X10-7 2 4 1.4X10-6 2 8 1.1X10-1 3 1 1. lxl〇-e 3 5 1.6Χ10-1 3 7 1.4Χ10-1 3 9 3. 4xl〇-7 4 1 4.3X10-1 4 3 2. 8X10-1 4 5 1. lxlO'6 4 7 6.9X10-1 5 1 1.4X10-7 5 3 1. 2X10-6 5 5 1.3xl〇-fl 5 7 3.4xl〇-7 氟苯桂畊 1.6x10-® (請先閲讀背面之注意事項再填寫本頁) 裝- ,1T. 本紙張尺度通用中界國家標準(CNS)甲4規格(210X297公*) -5?- 五、發明説明(58)
Λ 6 Β6 上 裝 脈 腿 大 於 後 醉 麻 納 妥 必 巴 戊 以 尤 成 MUM- 種 2 雜 例雄 驗雌 試 管測 套量 之流 用血 予以 投配 物脈 藥動 上骨 裝椎 脈於 靜乃 腿 , 大定 於測 及之 管量 套流 之血 用於 定 , 測者 壓再 血 〇 為 物 合 化 明 發 本 於 予 投 物 藥 ο 定 測 行 進 針 探 之 用 定 30 為 哄 桂 苯 氣 之 予表 投於 度示 濃化 低變 由之 中量 圍流 範血 (請先閲讀背面之注意事項再填寫本頁) 經濟部中央標準局貝工消費合作杜.子製 -60- 本紙張尺度逍用中國國家標準(CNS)甲4規格(210X297公*) 五、發明説明(59) 表2 k/«J·ο 5ο 66 ΑΒ 經濟部中央標準局貝工消费合作社卬製 化合物 港度 (/ig/kg, i. v.) 變化率 {%) 10 1〇_ 18: 30 14 100 80 300 125 3 5 10 13 . 30 26 100 66 300, 87 4 3 ία 7 30 15 100 55 300 131 4 1 ·. · · 10 12 30 25 100 66 300 8? 氟苯桂哄' 30 8 100 27 300 44 1000 55 (請先閲讀背面之注意事項再填寫本頁) 裝· 訂_ 本紙張反度逍用中國Η家標準(CNS)甲4規格(210X297公釐) 五、發明説明(60) A6 B6 經濟部中央標準局負工消費合作社卬製 試驗例3 急性毒性: 上述實施例所得之本發明二苯基哌阱衍生物之急性毒 性試驗以下列方法進行。 購入4週齡之ICR糸公鼠,約10天之預備飼育後供做 實驗。鼠於實驗前日1 6小時開始絶食。供試藥物溶解於 大豆油中使成鼠體重10克相當以0.2毫升並以金屬胃彎 探子(sonde)強制經口投予。另,對照組僅投予大豆油 。投予後之觀察期間為14天,並由14日後之生存率以 Litchfie 丨 d-Wilcoxon's法求得 LDso 值。 其結果,本發明之二苯基哌阱衍生物全部為lOOOmg/ k g以上。 製劑例1 1 化合物 I 2 4 . 0克 乳糖 I 5 I . I克 羥丙基纖維素 4. 9克 玉米澱粉 20.0克 合計 2 0 0 . 0克 化合物I ,乳糖及玉米澱粉以60號篩篩過並均勻混合後 ,置入練合機並加入羥丙基纖維素之水溶液練合。其次 ,由18號篩篩過者於50它下送風乾燥。乾燥後,整粒並 製成顆粒劑,分包成I包500毫克。 -62 - 本紙張尺度逍用中國Η家樣準(CNS)甲4規格(210X297公*) (請先閱讀背面之注意事項再填寫本頁) 裝- 訂_ Λ 6 Β6 五、發明説明(61) 製劑例 2 化合物 2 60.0克 乳糖 1 1 8 . 5克 玉米澱粉 2 0 . 0克 滑石 1 . 5克
經濟部中央標準局員工消費合作社卬U 合計 2 0 0 . 0克 磨 細 上 述 成 分 為 粉 末 » 充 分 攪 拌 成均 勻混 合 物 後,各 膠 囊 充 填 2克, 可得經口投予用之膠囊。 製 劑 例 3 化 合 物 3 60 .0克 乳 糖 113 • 1克 玉 米 澱 粉 20 •。克 羥 丙 基 m 維 素 4 .9克 硬 脂 酸 m 2 .0克 合 計 200 .0克 化 合 物 3, 乳糖及玉米澱粉以60號篩篩過並均勻混合 後 * 置 入 練 合 Uji 機 並 加 入 羥 丙 基 m 維 素之 水溶 液 練 合後, 於 50 V 下 送 風 乾 燥 〇 乾 燥 後 ♦ 通 過 16號 篩進 行 整 粒,並 均 勻 混 合 以 硬 脂 酸 m 参 以 打 錠 機 打 鍵而 得直 徑 8毫米, 重量200毫克之錠劑。 (請先閲讀背面之注意事項再填寫本頁) 裝- 訂_ 本紙張尺度逍用中國國家標準(CNS)甲4規格(210x297公*) Λ 6 Β 6 五、發明説明(62) 製劑例 4 化合物16 witepsol (H-15) witepsol (B-75) 6 . 0克 72 . 〇克 72 . 〇克 經濟部中央標準局員工消費合作社卬製 合計 1 5 0 , 0克 witepsol (H-15)與 witepsol (B-75)於 50-60*0 下混合 融解,在預先於乳缽内研和成徹細粉末之化合物3中一 邊攪拌一邊徐徐加入,充分混合均勻。於坐劑型中各注入 1.5克,於室溫放冷,可得固化坐劑。 製劑例 5 化合物 2 8 1 . 0克 0 . 1 N 鹽酸 10.0 克 C* i 苄醇 30.0克 注射用蒸餾水 適量 全量 1 000 . 0毫升 4 0 0毫升注射用蒸蹓水加至1 0毫升0 . 1 N鹽酸中,溶解 化合物5。於此溶液加人30毫升苄醇及適當之注射用蒸 腺水,以NaOH調整至PH3.0,全量為1000毫升充填於10 毫升安瓿中,進行高壓蒸氣殺菌可得注射劑。 産業上之利用可能性 -64- 本紙張尺度逍用中國國家標準(CNS)甲4規格(210x297公釐) (請先閱讀背面之注意事項再填寫本頁) 裝- 訂- 線· ^050^4 A 6 _B6_ 五、發明説明(63) 本發明之二苯基哌阱衍生物具有優異之鈣拮抗作用, 且副作用亦少。因此,以此為有效成分之循環器用藥, 為極有用於高血壓,狹心症,腦血流障礙,不整脈等循 環糸統疾病之治療及預防。 (請先閱讀背面之注意事項再填寫本頁) 裝- 訂- 經濟部中央標準局員工消費合作社印製 -65 - 冬紙張尺度逍用中a a家標準(CNS)甲4規格(210父297公龙)
Claims (1)
- 六、申請專利範圍 第80107221號r二苯基掀畊衍生物及其藥學組成物」專利案 (8 2年3月修正) 一種如下式(1)之二苯基哌畊衍生物或其鹽 OR3 r~\ I .Ηί.-,-Ν N-CH2CHCH2-Z-CnH2n-Ar (1) [式中,R1及R2可相同或相異各為氫原子,鹵原子* R3為氫原子,Ci - <烷基,醛基,Ar為可被1-2艏鹵 原子,Ci - +烷基,Ci - 4烷氧基,胺基,羥基所取代 之萘基或苯基,Z為硫原子或- N-(R+為氫原子,Ci - * 烷基),πι為1-5之整數,η為0-5之整數]。 .一種做為血流改善劑或鈣離子拮抗劑之藥學組成物,内 含如申謓專利範圍第1項之二苯基瞰畊衍生物或其豔為 有效成分。 .如申謓專利範圍第2項之藥學組成物,用以預防或治療高 血壓,狹心症或腦循琿障礙。 —裝------訂---卜— —線 (請先閲讀背面之注意事項再塡寫本頁) 經濟部中央標準局W工消费合作社印製
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0025111B1 (en) * | 1979-08-10 | 1984-07-25 | Sandoz Ag | 3-aminopropoxyaryl derivatives, their preparation and pharmaceutical compositions containing them |
| DE3200304A1 (de) * | 1981-01-16 | 1982-08-26 | Sandoz-Patent-GmbH, 7850 Lörrach | 3-aminopropoxyaryl-derivate, ihre herstellung und sie enthaltende arzneimittel |
| DE3600390A1 (de) * | 1986-01-09 | 1987-07-16 | Hoechst Ag | Diarylalkyl-substituierte alkylamine, verfahren zu ihrer herstellung, ihre verwendung sowie sie enthaltende arzneimittel |
| DE3723648A1 (de) * | 1987-07-17 | 1989-01-26 | Sandoz Ag | Indol-derivate, ihre herstellung und sie enthaltende arzneimittel |
| DE3831993A1 (de) * | 1988-09-21 | 1990-03-29 | Basf Ag | 2-hydroxy-3-phenoxy-propyl-substituierte piperazine und homo-piperazine, ihre herstellung und verwendung |
-
1991
- 1991-09-12 TW TW080107221A patent/TW205034B/zh active
- 1991-09-13 AU AU84916/91A patent/AU654969B2/en not_active Ceased
- 1991-09-13 US US07/988,911 patent/US5391552A/en not_active Expired - Fee Related
- 1991-09-13 CA CA002091248A patent/CA2091248C/en not_active Expired - Fee Related
- 1991-09-13 EP EP91915997A patent/EP0549796B1/en not_active Expired - Lifetime
- 1991-09-13 KR KR1019930700745A patent/KR0173141B1/ko not_active Expired - Fee Related
- 1991-09-13 WO PCT/JP1991/001227 patent/WO1992005165A1/ja not_active Ceased
- 1991-09-13 JP JP03515013A patent/JP3101677B2/ja not_active Expired - Fee Related
- 1991-09-13 AT AT91915997T patent/ATE165600T1/de not_active IP Right Cessation
- 1991-09-13 DE DE69129333T patent/DE69129333T2/de not_active Expired - Fee Related
- 1991-09-13 ES ES91915997T patent/ES2117013T3/es not_active Expired - Lifetime
- 1991-09-13 EP EP94104488A patent/EP0612738A1/en not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| EP0549796B1 (en) | 1998-04-29 |
| CA2091248C (en) | 2002-11-05 |
| ES2117013T3 (es) | 1998-08-01 |
| KR0173141B1 (ko) | 1999-02-01 |
| EP0549796A4 (en) | 1993-09-29 |
| CA2091248A1 (en) | 1992-03-14 |
| US5391552A (en) | 1995-02-21 |
| KR930702321A (ko) | 1993-09-08 |
| JP3101677B2 (ja) | 2000-10-23 |
| DE69129333D1 (de) | 1998-06-04 |
| EP0612738A1 (en) | 1994-08-31 |
| AU8491691A (en) | 1992-04-15 |
| ATE165600T1 (de) | 1998-05-15 |
| AU654969B2 (en) | 1994-12-01 |
| DE69129333T2 (de) | 1998-08-20 |
| EP0549796A1 (en) | 1993-07-07 |
| WO1992005165A1 (en) | 1992-04-02 |
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