Triethylamine → 4-[(8-cyclohexyloctyl)amino]-N-3-bromopropylbenzamide
반응식
[BrH:1].Br[CH:3]([CH3:6])[CH2:4][NH2:5].Cl.[CH:8]1([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][NH:22][C:23]2[CH:31]=[CH:30][C:26]([C:27](Cl)=[O:28])=[CH:25][CH:24]=2)[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1.C(N(CC)CC)C>CN(C)C1C=CN=CC=1.C(COC)OC>[CH:8]1([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][NH:22][C:23]2[CH:31]=[CH:30][C:26]([C:27]([NH:5][CH2:4][CH2:3][CH2:6][Br:1])=[O:28])=[CH:25][CH:24]=2)[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1참가 물질
6
실험 절차
To a slurry of 21.80 g. of 2-bromopropylamine hydrobromide in 200 ml. of glyme at 3° C. is added a solution of 23.96 g. of 4-(8-cyclohexyloctylamino)benzoyl chloride hydrochloride in 65 ml. of glyme, concurrently with 26 ml. of triethylamine diluted to 39 ml. with glyme. The solution is warmed to reflux and 0.2 g. of 4-dimethylaminopyridine is added. The solution is heated for four hours and cooled overnight. The solid is removed by filtration and the filtrate diluted with 200 ml. of water. The precipitate is collected and crystallized from cyclohexane. The solid is recrystallized from acetonitrile to yield the product.
후처리
- temperatureThe solution is warmed
- temperatureto reflux
- temperatureThe solution is heated for four hours
- temperaturecooled overnight
- customThe solid is removed by filtration
- additionthe filtrate diluted with 200 ml
- customThe precipitate is collected
- customcrystallized from cyclohexane
- customThe solid is recrystallized from acetonitrile
- customto yield the product
출처 및 근거
- ORD 기록
- ord-ba8d235a86664172a970eebf47ff6812
- 출처 데이터셋
- uspto-grants-1983_12
- 특허 번호
- US04423051
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