반응식
[N+:1]([N:4]=[C:5]1[NH:9][CH2:8][CH2:7][S:6]1)([O-:3])=[O:2].C(=O)([O-])[O-].[K+].[K+].[Cl:16][C:17]1[CH:22]=[CH:21][C:20]([CH2:23]Cl)=[CH:19][N:18]=1>C(#N)C>[Cl:16][C:17]1[CH:22]=[CH:21][C:20]([CH2:23][N:9]2[CH2:8][CH2:7][S:6][C:5]2=[N:4][N+:1]([O-:3])=[O:2])=[CH:19][N:18]=1참가 물질
5
실험 절차
A mixture of 2.9 g of 2-nitroiminothiazolidine, 2.9 g of anhydrous potassium carbonate, 3.2 g of 2-chloro-5-pyridylmethylchloride and 50 ml of acetonitrile was refluxed for 5 hours with vigorously stirring. After the reaction, most of the acetonitrile was removed by distillation and water was added to the residue. As the solid product was separated, it was collected by filtration. The crude material was recrystallized from ethanol to give desired 3-(2-chloro-5-pyridylmethyl)-2-(nitroimino)thiazolidine.
후처리
- temperaturewas refluxed for 5 hours
- customAfter the reaction
- custommost of the acetonitrile was removed by distillation and water
- additionwas added to the residue
- customAs the solid product was separated
- filtrationit was collected by filtration
- customThe crude material was recrystallized from ethanol
출처 및 근거
- ORD 기록
- ord-c5e117cc5b2245c587c08400dffad131
- 출처 데이터셋
- uspto-grants-2001_10
- 특허 번호
- US06297374B1
연결된 노트
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