Acetic Acid → Ammonia methanol dichloromethane

HRID 33698노트

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HRID 33698 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]=1

참가 물질

7

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

  1. customthe reaction was quenched with saturated aqueous sodium bicarbonate
  2. extractionthe aqueous phase was extracted with dichloromethane (120 mL)
  3. dry with materialThe organic phase was dried (magnesium sulfate)
  4. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-accdf9f94e824b48ab1a2eac8bb2b6b7
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07429586B2

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