SU530030A1 - Method for teaching amides of furancarboxylic acid - Google Patents
Method for teaching amides of furancarboxylic acidInfo
- Publication number
- SU530030A1 SU530030A1 SU2101345A SU2101345A SU530030A1 SU 530030 A1 SU530030 A1 SU 530030A1 SU 2101345 A SU2101345 A SU 2101345A SU 2101345 A SU2101345 A SU 2101345A SU 530030 A1 SU530030 A1 SU 530030A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- amides
- teaching
- furancarboxylic acid
- acid
- furancarboxylic
- Prior art date
Links
- 238000000034 method Methods 0.000 title description 6
- 150000001408 amides Chemical class 0.000 title description 3
- SMNDYUVBFMFKNZ-UHFFFAOYSA-N 2-furoic acid Chemical compound OC(=O)C1=CC=CO1 SMNDYUVBFMFKNZ-UHFFFAOYSA-N 0.000 title 1
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- OYMCMWPHMPODNK-UHFFFAOYSA-N 2-bromofuran Chemical compound BrC1=CC=CO1 OYMCMWPHMPODNK-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- TVFIYRKPCACCNL-UHFFFAOYSA-N furan-2-carboxamide Chemical class NC(=O)C1=CC=CO1 TVFIYRKPCACCNL-UHFFFAOYSA-N 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 208000024798 heartburn Diseases 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- -1 oxyl Chemical group 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
Landscapes
- Furan Compounds (AREA)
Description
Изобретение относитс к новому способу ползчени амидов фуранкарбоновой кислоты формулы IThis invention relates to a new creeping method for furancarboxylic acid amides of formula I
.0л.0l
,,
Р. ГН R. GN
ато:- вопороз-; ти -:етнл и R - атом зспопсла или галогена, метил, окси- лли Т1итрог;:г.лпз,atoms: - voporoz-; ti -: etnl and R - atom of spspl or halogen, methyl, oxyl T1 nitrog;
Соедкке-п-; этогг; класса обладают биологическ:; активными свойствами,Soedkke-p; this; class possess biological :; active properties
.г.-;СТ- C-i;ivCo6 мО -ченНГ: - феиИ,.g .-; CT-CI; ivCo6 MO-CHING: - fairies,
амид 2-фура;;карбоноъой кислоты, 2 кл-о-:аь: лийс в том, лто 2-бромфуран псдвергз- т присутствии йода, лолученный фурил-лагкийбгО л-л лоу1вергают взаимодействию с фенил .,а ..: 1J.amide 2-furan ;; carbonic acid, 2 C-o-: ai: liis, in that 2-bromo-furan is given by iodine, obtained by furyl-lagkybgO l-l low-volt interaction with phenyl ..
iV достатком этого способа вл етс iV prosperity of this method is
Muoi-остадийиый синтез w труднодост тгность исходных соединений.Muoi-ostadyny synthesis w hardness of the original compounds.
Известен также с .особ получени амидов фуранкарбсиовой кислоты, заключающийс в том, чго питзослизерлЮ KHCHOTV поцвсг/гают взаимодействию с хлористым тионилс.;.и полученный хлорангидрид пирослизевой кислоты подвергают взанмо.е;1ствию с a.xn:iном , например п-толуидином 2.i.A method for the preparation of amides of furancarbicic acid is also known, which consists in the pyclosis of the KHCHOTV cellulose g / g interacting with thionyl chloride; and the obtained pyros-lysic acid chloride is subjected to vamo. E; .i.
Недостатком этого способа в.л отс миогостадийный синтез и труднодосту:)П1ость х.;орангидридов ф фанкарбоновых клс.лотоThe disadvantage of this method is vl ots myo-stage synthesis and hard-to-stand:) P1ost h.; Orangidrides f fancarbon kls.lotto
Це.лью изобретени вл етсг; yiaOniemie процесса.The purpose of the invention is; yiaOniemie process.
Это достигаетс тем, чгг ф----ГО1 или сти.лфурфурол подвергают г-заг-.т сй::тви1с с лр: ;:2В.1Дным а;ц1лт1нп . .:стБии пере- F.ircfi во - роГЯ вст1ртовой среде при темпе-This is achieved by the fact that chgg s ---- GO1 or stiflfurol is subjected to g-zag-tt sy :: twi1s with lr:;: 2B.1Dnom a; c1lt1np. .: stBii pere- F.ircfi of the throes in an inert medium at a temperature
;;..- ,:-:; чени , под- с ;; ..-,: - :; cheni
R- 4i iUcHo ,R-4i iUcHo,
J- ;-:- Hiibf JH; eтcи . з nuijJ-; -: - Hiibf JH; ets. s nuij
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU2101345A SU530030A1 (en) | 1975-01-24 | 1975-01-24 | Method for teaching amides of furancarboxylic acid |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU2101345A SU530030A1 (en) | 1975-01-24 | 1975-01-24 | Method for teaching amides of furancarboxylic acid |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU530030A1 true SU530030A1 (en) | 1976-09-30 |
Family
ID=20608859
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU2101345A SU530030A1 (en) | 1975-01-24 | 1975-01-24 | Method for teaching amides of furancarboxylic acid |
Country Status (1)
| Country | Link |
|---|---|
| SU (1) | SU530030A1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8119811B2 (en) | 2007-04-11 | 2012-02-21 | Sumitomo Chemical Company, Limited | Method for producing amide compound |
-
1975
- 1975-01-24 SU SU2101345A patent/SU530030A1/en active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8119811B2 (en) | 2007-04-11 | 2012-02-21 | Sumitomo Chemical Company, Limited | Method for producing amide compound |
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