GB548626A - Substituted ureas - Google Patents
Substituted ureasInfo
- Publication number
- GB548626A GB548626A GB44241A GB44241A GB548626A GB 548626 A GB548626 A GB 548626A GB 44241 A GB44241 A GB 44241A GB 44241 A GB44241 A GB 44241A GB 548626 A GB548626 A GB 548626A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diethylamide
- carboxylic
- nhr
- alike
- bis
- 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
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
- C07D295/215—Radicals derived from nitrogen analogues of carbonic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/04—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms
- C07C275/06—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms of an acyclic and saturated carbon skeleton
- C07C275/14—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms of an acyclic and saturated carbon skeleton being further substituted by nitrogen atoms not being part of nitro or nitroso groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
548,626. Substituted ureas. BOON, W. R., and IMPERIAL CHEMICAL INDUSTRIES, Ltd. Jan. 13, 1941, No. 442. [Class 2 (iii)] Alkylene bis-ureas, X.CO.NR<SP>1</SP>.(CH 2 ) n .NR<SP>11</SP>- COY, where X and Y which may be alike are radicals of secondary aliphatic or heterocyclic secondary amines having a molecular weight not exceeding 120, R<SP>1</SP> and R<SP>11</SP> are alkyl groups not necessarily alike and which jointly contain not more than 8 carbon atoms, and n is 2 to 6, are prepared bv treating a mono-urea X.CO.- NR<SP>1</SP>.(CH 2 ) n .NHR<SP>11</SP> with a carbamyl chloride Y.COCl, or with phosgene to form a carbamyl chloride which is then treated with an aliphatic or heterocyclic secondary amine. When X and Y are alike the products are the same as those of Specification 548,625. Examples give the preparation of N:N<SP>1</SP>-dimethyltrimethylenediamine-N:N<SP>1</SP>-dicarboxylic bis-diethylamide, - N-carboxylic diethylamide-N<SP>1</SP>-carboxylic dimethylamide, and -N-carboxylic diethylamide- N<SP>1</SP>-carboxylic piperidide, N:N<SP>1</SP> - dimethylhexamethylene-N:N '-dicarboxylic bis-diethylamide and-N-carboxylic diethylamide-N<SP>1</SP>-carboxylic morpholide, and N:N<SP>1</SP>-diethylethylene-N:N<SP>1</SP>- dicarboxylic bis-diethylamide. Mono-ureas, X.CO.NR<SP>1</SP>.(CH 2 ) n .NHR<SP>11</SP> are prepared by causing a N:N<SP>1</SP>-dialkylalkylenediamine, NHR<SP>1</SP>.(CH 2 ) n NHR<SP>11</SP> to react with one molecular proportion of a carbamyl chloride Y.COCl. Examples are N:N<SP>1</SP>-dimethyltrimethylene- and -diethylethylene-diamine-N-carboxylic diethylamide.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB44241A GB548626A (en) | 1941-01-13 | 1941-01-13 | Substituted ureas |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB44241A GB548626A (en) | 1941-01-13 | 1941-01-13 | Substituted ureas |
Publications (1)
Publication Number | Publication Date |
---|---|
GB548626A true GB548626A (en) | 1942-10-19 |
Family
ID=9704404
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB44241A Expired GB548626A (en) | 1941-01-13 | 1941-01-13 | Substituted ureas |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB548626A (en) |
-
1941
- 1941-01-13 GB GB44241A patent/GB548626A/en not_active Expired
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