Acetic Acid → Ammonia methanol dichloromethane
반응식
Cl.[N:2]1([CH2:7][CH2:8][CH2:9][O:10][C:11]2[CH:16]=[CH:15][C:14]([N:17]3[CH2:22][CH2:21][NH:20][CH2:19][CH2:18]3)=[CH:13][CH:12]=2)[CH2:6][CH2:5][CH2:4][CH2:3]1.[CH:23](=O)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.C(O)(=O)C.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].[Cl:49][CH:50]([Cl:52])C>>[NH3:2].[CH3:9][OH:10].[Cl:49][CH2:50][Cl:52].[CH2:23]([N:20]1[CH2:19][CH2:18][N:17]([C:14]2[CH:13]=[CH:12][C:11]([O:10][CH2:9][CH2:8][CH2:7][N:2]3[CH2:6][CH2:5][CH2:4][CH2:3]3)=[CH:16][CH:15]=2)[CH2:22][CH2:21]1)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1참가 물질
7
반응물 5
생성물 2
실험 절차
A solution of the product of Example 23 (148 mg), benzaldehyde (520 mg), and acetic acid (25 mg) in dichloroethane (3 mL) was treated with sodium triacetoxyborohydride (121 mg). After 14 h, the reaction was quenched with saturated aqueous sodium bicarbonate, and the aqueous phase was extracted with dichloromethane (120 mL). The organic phase was dried (magnesium sulfate) and evaporated in vacuo. Silica gel chromatography of the residue (5% 2M ammonia-methanol/dichloromethane) gave the title compound as a light yellow solid (8 mg). 1H NMR (400 MHz, CDCl3): 7.36-7.24 (m, 5H), 6.94-6.81 (m, 4H), 3.96 (t, J=6.4 Hz, 2H), 3.56 (s, 2H), 3.08 (t, J=4.9 Hz, 4H), 2.64-2.60 (m, 4H), 2.04-1.94 (m, 2H), 1.80-1.75 (m, 4H).
후처리
- customthe reaction was quenched with saturated aqueous sodium bicarbonate
- extractionthe aqueous phase was extracted with dichloromethane (120 mL)
- dry with materialThe organic phase was dried (magnesium sulfate)
- customevaporated in vacuo
출처 및 근거
- ORD 기록
- ord-accdf9f94e824b48ab1a2eac8bb2b6b7
- 출처 데이터셋
- uspto-grants-2008_09
- 특허 번호
- US07429586B2
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