반응식
Cl.[CH2:2]([O:4][C:5](=[O:10])[CH2:6][C:7](=[NH:9])[NH2:8])[CH3:3].[O-]CC.[Na+].Br[CH2:16][C:17]([C:19]1[CH:26]=[CH:25][C:22]([C:23]#[N:24])=[CH:21][CH:20]=1)=O>C(O)C>[CH2:2]([O:4][C:5]([C:6]1[CH:16]=[C:17]([C:19]2[CH:26]=[CH:25][C:22]([C:23]#[N:24])=[CH:21][CH:20]=2)[NH:9][C:7]=1[NH2:8])=[O:10])[CH3:3]참가 물질
반응 조건
- 온도
- 2.5 °C
실험 절차
A mixture of 42.53 g (0.255 mol) carbamimidoyl-acetic acid ethyl ester hydrochloride in 70 ml absolute ethanol is treated at 0 to 5° C. with 95.3 ml of a 21% sodium ethoxide solution in ethanol (0.255 mol) and stirred 5 min at 0 to 5° C. 4-Bromoacetyl-benzonitrile (28.6 g, 0.128 mol) is then added in portions over 20 min at 0 to 5° C. Stirring is continued at this temperature for 5 min then the ice bath is removed and the yellow suspension is stirred over night at RT. The solid is filtered off, washed with ethanol and ether and re-suspended in 450 ml actonitrile. The mixture is heated for 5 min under reflux, filtered while still hot and then cooled in an ice bath. The title compound is collected by succion and dried. Flash chromatography (dichtoromethane/ethyl acetate mixture) of the mother liquors gives an additional crop of the title compound as a yellow solid; m.p. 228-229° C.; MS-ES+: (M+H)+=254.
후처리
- stirringStirring
- waitis continued at this temperature for 5 min
- customthe ice bath is removed
- stirringthe yellow suspension is stirred over night at RT
- filtrationThe solid is filtered off
- washwashed with ethanol and ether
- temperatureThe mixture is heated for 5 min
- temperatureunder reflux
- filtrationfiltered while still hot and
- temperaturethen cooled in an ice bath
- customThe title compound is collected by succion
- customdried
출처 및 근거
- ORD 기록
- ord-8e8d411034a346a3b031889df9058a94
- 출처 데이터셋
- uspto-grants-2008_06
- 특허 번호
- US07390805B2
연결된 노트
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