FR2424262A1 - Anti-tremor and anti-anxiety malonylurea tetramer complex cpds. - prepd. by reacting barbiturate derivs. with n-substd. barbituric acid cpds. (BE 2.5.78) - Google Patents
Anti-tremor and anti-anxiety malonylurea tetramer complex cpds. - prepd. by reacting barbiturate derivs. with n-substd. barbituric acid cpds. (BE 2.5.78)Info
- Publication number
- FR2424262A1 FR2424262A1 FR7812042A FR7812042A FR2424262A1 FR 2424262 A1 FR2424262 A1 FR 2424262A1 FR 7812042 A FR7812042 A FR 7812042A FR 7812042 A FR7812042 A FR 7812042A FR 2424262 A1 FR2424262 A1 FR 2424262A1
- Authority
- FR
- France
- Prior art keywords
- cpds
- malonylurea
- derivs
- substd
- prepd
- 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.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/60—Three or more oxygen or sulfur atoms
- C07D239/62—Barbituric acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
New malonylurea derivs. are complexes of formula (I). In this formula, R1 and R2 are -CH2CHAB in which A is H and B is OH, or A is -CH2OX (X = H or 1-5C alkyl) adn B is -OY (Y = H, opt. substd. carbamol, or carbalkoxy); R3, R4, R5, R6, R7 and R8 are H or aliphatic, araliphatic or aryl and the broken lines indicate H bonds. Unlike the barbiturates to which tey are related, (I) have minimal hypnotic activity, low toxicity, and reduced risk of addiction. Specific. complexes (I) inlcude those in which R1 and R2 are each -CH2CH(OCONH2)-CH2OCH-CH3)2, R3, R5 and R7 are ethyl, and R4, R6 and R8 are phenyl. In an example, this is prepd. by mixing phenobarbital, 5-ethyl-5-phenyl-N-(3-isopropoxy-2-carbamoyloxypropyl)malonylure and 5-ethyl-5-phenyl-N-N'-di-(3-isopropoxy-2-carbamoyloxypropyl)maloy- lurea in a molar ratio of 1:2:1 in a mortar, melting the mixture, and pouring the melt into water.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR7812042A FR2424262A1 (en) | 1978-04-24 | 1978-04-24 | Anti-tremor and anti-anxiety malonylurea tetramer complex cpds. - prepd. by reacting barbiturate derivs. with n-substd. barbituric acid cpds. (BE 2.5.78) |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR7812042A FR2424262A1 (en) | 1978-04-24 | 1978-04-24 | Anti-tremor and anti-anxiety malonylurea tetramer complex cpds. - prepd. by reacting barbiturate derivs. with n-substd. barbituric acid cpds. (BE 2.5.78) |
Publications (2)
Publication Number | Publication Date |
---|---|
FR2424262A1 true FR2424262A1 (en) | 1979-11-23 |
FR2424262B1 FR2424262B1 (en) | 1981-05-22 |
Family
ID=9207508
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR7812042A Granted FR2424262A1 (en) | 1978-04-24 | 1978-04-24 | Anti-tremor and anti-anxiety malonylurea tetramer complex cpds. - prepd. by reacting barbiturate derivs. with n-substd. barbituric acid cpds. (BE 2.5.78) |
Country Status (1)
Country | Link |
---|---|
FR (1) | FR2424262A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0125046A1 (en) * | 1983-04-12 | 1984-11-14 | Sapos S.A. | Process for preparing pyrimidinetrione derivatives |
WO1991012244A1 (en) * | 1990-02-08 | 1991-08-22 | Sapos S.A. | Process for preparing pyrimidinetrione derivatives |
US11072588B2 (en) * | 2017-03-31 | 2021-07-27 | Universitetet I Tromsø—Norges Arktiske Universitet | Barbituric acid derivatives comprising cationic and lipophilic groups |
-
1978
- 1978-04-24 FR FR7812042A patent/FR2424262A1/en active Granted
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0125046A1 (en) * | 1983-04-12 | 1984-11-14 | Sapos S.A. | Process for preparing pyrimidinetrione derivatives |
AT388917B (en) * | 1983-04-12 | 1989-09-25 | Sapos Sa | METHOD FOR PRODUCING PYRIMID INTRION DERIVATIVES |
WO1991012244A1 (en) * | 1990-02-08 | 1991-08-22 | Sapos S.A. | Process for preparing pyrimidinetrione derivatives |
US5262402A (en) * | 1990-02-08 | 1993-11-16 | Sapos S.A. | Process for preparing pyrimidinetrione derivatives |
US11072588B2 (en) * | 2017-03-31 | 2021-07-27 | Universitetet I Tromsø—Norges Arktiske Universitet | Barbituric acid derivatives comprising cationic and lipophilic groups |
Also Published As
Publication number | Publication date |
---|---|
FR2424262B1 (en) | 1981-05-22 |
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