FR2147953A1 - 2-hydroxy-phenylethyl guanidines and their alkyl ethers - useful as hypotensives and antihypertensives - Google Patents
2-hydroxy-phenylethyl guanidines and their alkyl ethers - useful as hypotensives and antihypertensivesInfo
- Publication number
- FR2147953A1 FR2147953A1 FR7223195A FR7223195A FR2147953A1 FR 2147953 A1 FR2147953 A1 FR 2147953A1 FR 7223195 A FR7223195 A FR 7223195A FR 7223195 A FR7223195 A FR 7223195A FR 2147953 A1 FR2147953 A1 FR 2147953A1
- Authority
- FR
- France
- Prior art keywords
- hypotensives
- antihypertensives
- guanidines
- phenylethyl
- hydroxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- KNWYGUHUNHVZSW-UHFFFAOYSA-N 2-[2-(2-hydroxyphenyl)ethyl]guanidine Chemical class NC(N)=NCCC1=CC=CC=C1O KNWYGUHUNHVZSW-UHFFFAOYSA-N 0.000 title 1
- 208000001953 Hypotension Diseases 0.000 title 1
- 150000005215 alkyl ethers Chemical class 0.000 title 1
- 229940030600 antihypertensive agent Drugs 0.000 title 1
- 239000002220 antihypertensive agent Substances 0.000 title 1
- 208000021822 hypotensive Diseases 0.000 title 1
- 230000001077 hypotensive effect Effects 0.000 title 1
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 abstract 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 abstract 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 abstract 1
- 229910010084 LiAlH4 Inorganic materials 0.000 abstract 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 abstract 1
- BHHGXPLMPWCGHP-UHFFFAOYSA-N Phenethylamine Chemical compound NCCC1=CC=CC=C1 BHHGXPLMPWCGHP-UHFFFAOYSA-N 0.000 abstract 1
- 238000005915 ammonolysis reaction Methods 0.000 abstract 1
- 230000003276 anti-hypertensive effect Effects 0.000 abstract 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- ZIPLUEXSCPLCEI-UHFFFAOYSA-N iminomethylideneazanide Chemical compound [NH-]C#N ZIPLUEXSCPLCEI-UHFFFAOYSA-N 0.000 abstract 1
- 239000012280 lithium aluminium hydride Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C45/70—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form
- C07C45/71—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form being hydroxy groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Anti-hypertensive title cpds. of formula (I):- (n = 0-4) and salts of (I), are prepd. by (a) condensing a phenyl-ethylamine with H2NC triple bond N or H2NC(=NH)Y, where Y is a labile gp. e.g. l.S-alkyl; (b) ammonolysis of the cyanoamide, iso-thiourea etc. derivs. of (I); (c) by reducing the corres. urethane with LiAlH4, or (d) by condensing guanidine with a reactive ester of the phenylethanol.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15810571A | 1971-06-29 | 1971-06-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| FR2147953A1 true FR2147953A1 (en) | 1973-03-11 |
Family
ID=22566703
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FR7223195A Withdrawn FR2147953A1 (en) | 1971-06-29 | 1972-06-27 | 2-hydroxy-phenylethyl guanidines and their alkyl ethers - useful as hypotensives and antihypertensives |
Country Status (8)
| Country | Link |
|---|---|
| JP (1) | JPS4856638A (en) |
| AU (1) | AU4392272A (en) |
| BE (1) | BE785522A (en) |
| DE (1) | DE2229931A1 (en) |
| FR (1) | FR2147953A1 (en) |
| IL (1) | IL39673A0 (en) |
| NL (1) | NL7208961A (en) |
| ZA (1) | ZA724018B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1988000181A1 (en) * | 1986-06-26 | 1988-01-14 | Harbor Branch Oceanographic Institution, Inc. | Antiviral guanidine derivative compositions and their methods of use |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3312516A1 (en) * | 1983-04-07 | 1984-10-11 | Brigitte Dr. 7400 Tübingen Pfeiffer | CORE-SUBSTITUTED PHENYLALKYLENGUANIDE DERIVATIVES, PROCESS FOR THEIR PRODUCTION AND MEDICINAL PRODUCTS CONTAINING THE SAME |
| JP2717916B2 (en) * | 1993-05-11 | 1998-02-25 | 日本化成株式会社 | Method for removing carbon adhering to riser in coke oven |
| US8846955B2 (en) | 2009-08-24 | 2014-09-30 | National Institute Of Information And Communications Technology | Second-order nonlinear optical compound and nonlinear optical element comprising the same |
-
1972
- 1972-06-12 IL IL39673A patent/IL39673A0/en unknown
- 1972-06-12 ZA ZA724018A patent/ZA724018B/en unknown
- 1972-06-20 DE DE2229931A patent/DE2229931A1/en active Pending
- 1972-06-27 FR FR7223195A patent/FR2147953A1/en not_active Withdrawn
- 1972-06-27 AU AU43922/72A patent/AU4392272A/en not_active Expired
- 1972-06-28 BE BE785522A patent/BE785522A/en unknown
- 1972-06-28 NL NL7208961A patent/NL7208961A/xx unknown
- 1972-06-28 JP JP47064176A patent/JPS4856638A/ja active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1988000181A1 (en) * | 1986-06-26 | 1988-01-14 | Harbor Branch Oceanographic Institution, Inc. | Antiviral guanidine derivative compositions and their methods of use |
Also Published As
| Publication number | Publication date |
|---|---|
| BE785522A (en) | 1972-12-28 |
| ZA724018B (en) | 1973-07-25 |
| DE2229931A1 (en) | 1973-01-18 |
| NL7208961A (en) | 1973-01-03 |
| JPS4856638A (en) | 1973-08-09 |
| IL39673A0 (en) | 1972-08-30 |
| AU4392272A (en) | 1974-01-03 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| ST | Notification of lapse |