GB1343426A - Acylated lactams - Google Patents
Acylated lactamsInfo
- Publication number
- GB1343426A GB1343426A GB1343426DA GB1343426A GB 1343426 A GB1343426 A GB 1343426A GB 1343426D A GB1343426D A GB 1343426DA GB 1343426 A GB1343426 A GB 1343426A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- acylated lactams
- lactam
- heading
- alkenyl
- 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
- C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
- C07D223/02—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D223/06—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings 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
- C07D223/08—Oxygen atoms
- C07D223/10—Oxygen atoms attached in position 2
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
1343426 N-Acylated lactams DOW CORNING Ltd 7 May 1971 [4 May 1970] 21376/70 Heading C2C [Also in Division C3] Compounds of the formula wherein R represents a C 3-18 alkenyl or alkynyl radical and R<SP>1</SP> represents a C 2-15 alkylene radical, may be obtained by reacting under substantially anhydrous conditions a compound of formula RCOCl with a lactam of formula wherein X represents hydrogen, an alkali metal atom, or a trihydrocarbylsilyl group. The reaction is suitably effected in a solvent, optionally in the presence of an acid acceptor.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2137670 | 1971-05-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1343426A true GB1343426A (en) | 1974-01-10 |
Family
ID=10161879
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1343426D Expired GB1343426A (en) | 1971-05-07 | 1971-05-07 | Acylated lactams |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1343426A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4755535A (en) * | 1986-04-23 | 1988-07-05 | Nelson Research & Development Co. | Compositions comprising 1-substituted azacycloalkenes |
US4801586A (en) * | 1986-04-23 | 1989-01-31 | Nelson Research & Development Co. | Penetration enhancers for transdermal delivery of systemic agents |
EP0368933A4 (en) * | 1987-09-30 | 1990-03-28 | Whitby Res Inc | Compositions comprising 1-oxo- or thiohydrocarbyl substituted azacycloalkanes. |
EP0416034A1 (en) * | 1988-05-27 | 1991-03-13 | NELSON RESEARCH & DEVELOPMENT CO. | Penetration enhancers for transdermal delivery of systemic agent |
EP0552504A1 (en) * | 1992-01-20 | 1993-07-28 | Schwarz Pharma Ag | Pharmaceutical compositions containing 1-oleylazacycloheptan-2-one as enhancing agent of transport across biological membranes |
EP0789689A1 (en) * | 1994-11-03 | 1997-08-20 | The Procter & Gamble Company | Process for the production of acyl lactams |
-
1971
- 1971-05-07 GB GB1343426D patent/GB1343426A/en not_active Expired
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4755535A (en) * | 1986-04-23 | 1988-07-05 | Nelson Research & Development Co. | Compositions comprising 1-substituted azacycloalkenes |
US4801586A (en) * | 1986-04-23 | 1989-01-31 | Nelson Research & Development Co. | Penetration enhancers for transdermal delivery of systemic agents |
EP0368933A4 (en) * | 1987-09-30 | 1990-03-28 | Whitby Res Inc | Compositions comprising 1-oxo- or thiohydrocarbyl substituted azacycloalkanes. |
EP0368933A1 (en) * | 1987-09-30 | 1990-05-23 | Whitby Research Incorporated | Compositions comprising 1-oxo- or thiohydrocarbyl substituted azacycloalkanes |
EP0416034A1 (en) * | 1988-05-27 | 1991-03-13 | NELSON RESEARCH & DEVELOPMENT CO. | Penetration enhancers for transdermal delivery of systemic agent |
EP0416034A4 (en) * | 1988-05-27 | 1992-04-01 | Nelson Research & Development Co. | Penetration enhancers for transdermal delivery of systemic agent |
EP0552504A1 (en) * | 1992-01-20 | 1993-07-28 | Schwarz Pharma Ag | Pharmaceutical compositions containing 1-oleylazacycloheptan-2-one as enhancing agent of transport across biological membranes |
EP0789689A1 (en) * | 1994-11-03 | 1997-08-20 | The Procter & Gamble Company | Process for the production of acyl lactams |
EP0789689A4 (en) * | 1994-11-03 | 1998-02-25 | Procter & Gamble | Process for the production of acyl lactams |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |