Hydrochloric Acid → 1-Benzoyl-3-[1-(2-[1,4-benzodioxan-2-yl]-2-hydroxyethyl)piperid-4-yl]-urea
반응식
[C:1]([NH:9][C:10]([NH:12][CH:13]1[CH2:18][CH2:17][N:16]([CH2:19][C:20]([CH:22]2[O:27][C:26]3[CH:28]=[CH:29][CH:30]=[CH:31][C:25]=3[O:24][CH2:23]2)=[O:21])[CH2:15][CH2:14]1)=[O:11])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[BH4-].[Na+].O.Cl>CO.[OH-].[Na+]>[C:1]([NH:9][C:10]([NH:12][CH:13]1[CH2:14][CH2:15][N:16]([CH2:19][CH:20]([CH:22]2[O:27][C:26]3[CH:28]=[CH:29][CH:30]=[CH:31][C:25]=3[O:24][CH2:23]2)[OH:21])[CH2:17][CH2:18]1)=[O:11])(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
1-Benzoyl-3-[1-(2-[1,4-benzodioxan-2-yl]-2-oxoethyl)piperid-4-yl]-urea (7.21 g, 0.017 mol) was suspended in methanol (80 cm3) and was stirred at room temperature. Sodium borohydride (1.0 g, 0.026 mol) in 2N sodium hydroxide (10 cm3) was added dropwise to the stirring solution and then left to stir for a further hour. Water was added and the solid filtered off and dried (5.41 g, 75%). A. T.L.C. of a small portion of the solid was run in freshly prepared toluene: ethanol: 0.880 ammonia (90:10:1 by volume) on a silica plate and was found to contain two components having RF values of about 0.30 and 0.34. The solid was recrystallised from n-butyl acetate (9 times) to give the component (1.19 g) with the lower RF value. This was suspended in a small amount of methanol and ethanolic HCl added until the solution was just acidic. The hydrochloride of the title compound (0.96 g, 74%) was collected.
후처리
- waitleft
- stirringto stir for a further hour
- filtrationthe solid filtered off
- customdried (5.41 g, 75%)
- customThe solid was recrystallised from n-butyl acetate (9 times)
- customto give the component (1.19 g) with the lower RF value
- additionadded until the solution
- customThe hydrochloride of the title compound (0.96 g, 74%) was collected
출처 및 근거
- ORD 기록
- ord-0309968e12cb464eb994a24632eb2221
- 출처 데이터셋
- uspto-grants-1980_11
- 특허 번호
- US04235915
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