Acetic Acid → 3-(1-ethoxycarbonylnonylamino)-5-t-butoxycarbonylmethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one
반응식
[NH2:1][CH:2]1[C:8](=[O:9])[N:7]([CH2:10][C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])[C:6]2[CH:18]=[CH:19][CH:20]=[CH:21][C:5]=2[S:4][CH2:3]1.O=[C:23]([CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36])[C:24]([O:26][CH2:27][CH3:28])=[O:25].C(O)(=O)C.[BH]C#N.[Na]>C(O)C>[CH2:27]([O:26][C:24]([CH:23]([NH:1][CH:2]1[C:8](=[O:9])[N:7]([CH2:10][C:11]([O:13][C:14]([CH3:16])([CH3:17])[CH3:15])=[O:12])[C:6]2[CH:18]=[CH:19][CH:20]=[CH:21][C:5]=2[S:4][CH2:3]1)[CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH3:36])=[O:25])[CH3:28]참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
1.3 g of 3-amino-5-t-butoxycarbonylmethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one and 3.0 g of ethyl 2-ketodecanoate were dissolved in 10 ml of ethanol. After the addition of 0.3 ml of acetic acid, the resulting mixture was stirred for 3 hours. Then, a solution of 420 mg of sodium boron cyanide hydride in 7 ml of ethanol was added dropwise thereto. After this mixture was allowed to stand overnight, it was concentrated under reduced pressure and the residue was dissolved in ethyl acetate. The solution was washed with water, dried and then concentrated. The residue was purified by silica gel column chromatography using a 7:1 mixture of benzene and ethyl acetate as the eluent. Thus, there was obtained 1.8 g of the desired compound in the form of an oily material.
후처리
- waitto stand overnight
- concentrationit was concentrated under reduced pressure
- dissolutionthe residue was dissolved in ethyl acetate
- washThe solution was washed with water
- customdried
- concentrationconcentrated
- customThe residue was purified by silica gel column chromatography
- additiona 7:1 mixture of benzene and ethyl acetate as the eluent
출처 및 근거
- ORD 기록
- ord-835edb2ab3ce49f6b9b50ad7e09e8967
- 출처 데이터셋
- uspto-grants-1985_09
- 특허 번호
- US04539150
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