GB1307028A - Phenethylamide derivatives and a process for the manufacture thereof - Google Patents
Phenethylamide derivatives and a process for the manufacture thereofInfo
- Publication number
- GB1307028A GB1307028A GB5033171A GB5033171A GB1307028A GB 1307028 A GB1307028 A GB 1307028A GB 5033171 A GB5033171 A GB 5033171A GB 5033171 A GB5033171 A GB 5033171A GB 1307028 A GB1307028 A GB 1307028A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- group
- acid
- boric acid
- compound
- 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.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
- C07D207/273—2-Pyrrolidones with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to other ring carbon atoms
- C07D207/277—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D207/28—2-Pyrrolidone-5- carboxylic acids; Functional derivatives thereof, e.g. esters, nitriles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
1307028 3,4 - Dihydroxyphenylethylamine derivatives and boric acid complexes thereof F HOFFMANN-LA ROCHE & CO AG 29 Oct 1971 [30 Oct 1970] 50331/71 Headings C2B and C2C Novel compounds of Formula I wherein R represents a C 1-8 t-alkoxycarbonyl group, a 5-oxo-2-pyrrolidinecarbonyl group, a phenylsulphonyl group which may be C 1-7 alkyl-substituted or a nitro-substituted phenylthio group, and salts thereof are prepared by one of the following methods - (a) by acidic hydrolysis of a boric acid complex of the compound of Formula I above, (b) by dibenzylating a compound of Formula II wherein R<SP>1</SP> is a C 1-8 t-alkoxycarbonyl group, a N - benzyloxycarbonyl - 5 - oxo - 2 - pyrrolidinecarbonyl group or a phenylsulphonyl group which may be C 1-7 alkyl substituted, and (c) by mild basic hydrolysis of a compound of formula wherein R<SP>11</SP> is a C 1-8 t-alkoxycarbonyl group and R 1 is C 1-7 alkyl or phenyl. 0,0<SP>1</SP> - Nitrophenyldisulphide is obtained as a by-product from the acid hydrolysis of the boric acid complex of N-[(o-nitrophenyl)thio]- dopamine by method (a) above. Intermediates of Formula II above are prepared by reacting 3,4-dibenzyloxyphenethylamine or a salt thereof with an agent furnishing the group R<SP>1</SP>, e.g. p-toluene sulphonyl chloride or N-carbobenzyloxy-L-pyroglutamic acid dicyclohexylamine salt. Boric acid complexes of compounds of Formula I above are prepared by treating a solution of dopamine of Formula IV or a salt thereof with boric, acid or a borate at a pH of at least 7 to form a boric acid complex of the dopamine of the Formula IV in which the two phenolic hydroxy groups are esterified with boric acid and then treating this di-borate ester with an agent furnishing the radical R such as an acid halide, acid anhydride or acid azide particularly t-butoxycarbonyl azide. Pharmaceutical compositions in conventional forms for enteral or parenteral administration having hypotensive, - antipyretic and anti- Parkinson activity comprise an above novel compound I and a carrier therefor.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH1604470A CH540230A (en) | 1970-10-30 | 1970-10-30 | Process for the production of phenethylamides |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1307028A true GB1307028A (en) | 1973-02-14 |
Family
ID=4414026
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB5033171A Expired GB1307028A (en) | 1970-10-30 | 1971-10-29 | Phenethylamide derivatives and a process for the manufacture thereof |
Country Status (10)
Country | Link |
---|---|
AU (1) | AU3357971A (en) |
BE (1) | BE774674A (en) |
CA (1) | CA958020A (en) |
CH (2) | CH544070A (en) |
DE (1) | DE2153825A1 (en) |
FR (1) | FR2111950B1 (en) |
GB (1) | GB1307028A (en) |
IL (1) | IL37702A (en) |
NL (1) | NL7113513A (en) |
ZA (1) | ZA716133B (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4443473A (en) * | 1981-06-30 | 1984-04-17 | The Procter & Gamble Company | Carbamate derivatives |
DE102007035642A1 (en) * | 2007-07-30 | 2009-02-12 | Grietje Beck | Substances for protecting cells and tissues against damage due to unfavorable conditions |
-
1970
- 1970-10-30 CH CH369273A patent/CH544070A/en unknown
- 1970-10-30 CH CH1604470A patent/CH540230A/en not_active IP Right Cessation
-
1971
- 1971-09-13 IL IL37702A patent/IL37702A/en unknown
- 1971-09-13 ZA ZA716133A patent/ZA716133B/en unknown
- 1971-09-16 AU AU33579/71A patent/AU3357971A/en not_active Expired
- 1971-10-01 NL NL7113513A patent/NL7113513A/xx unknown
- 1971-10-22 CA CA125,840A patent/CA958020A/en not_active Expired
- 1971-10-28 DE DE19712153825 patent/DE2153825A1/en active Pending
- 1971-10-28 FR FR7138782A patent/FR2111950B1/fr not_active Expired
- 1971-10-29 GB GB5033171A patent/GB1307028A/en not_active Expired
- 1971-10-29 BE BE774674A patent/BE774674A/en unknown
Also Published As
Publication number | Publication date |
---|---|
IL37702A0 (en) | 1971-11-29 |
CH540230A (en) | 1973-08-15 |
AU3357971A (en) | 1973-03-22 |
ZA716133B (en) | 1972-06-28 |
BE774674A (en) | 1972-05-02 |
CH544070A (en) | 1973-11-15 |
FR2111950B1 (en) | 1975-04-18 |
NL7113513A (en) | 1972-05-03 |
CA958020A (en) | 1974-11-19 |
DE2153825A1 (en) | 1972-05-04 |
IL37702A (en) | 1975-02-10 |
FR2111950A1 (en) | 1972-06-09 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed [section 19, patents act 1949] | ||
PLNP | Patent lapsed through nonpayment of renewal fees |