N,O-Dimethylhydroxylamine → 1-({5-[(diallylamino)methyl]thien-2-yl}sulfonyl)-N-methoxy-N-methylpiperidine-4-carboxamide

HRID 906643노트

반응식

HRID 906643 반응식
[CH2:1]([N:4]([CH2:8][C:9]1[S:13][C:12]([S:14]([N:17]2[CH2:22][CH2:21][CH:20]([C:23](OC)=[O:24])[CH2:19][CH2:18]2)(=[O:16])=[O:15])=[CH:11][CH:10]=1)[CH2:5][CH:6]=[CH2:7])[CH:2]=[CH2:3].[CH3:27][NH:28][O:29][CH3:30].C([Mg]Cl)(C)C>C1COCC1>[CH2:1]([N:4]([CH2:8][C:9]1[S:13][C:12]([S:14]([N:17]2[CH2:22][CH2:21][CH:20]([C:23]([N:28]([O:29][CH3:30])[CH3:27])=[O:24])[CH2:19][CH2:18]2)(=[O:15])=[O:16])=[CH:11][CH:10]=1)[CH2:5][CH:6]=[CH2:7])[CH:2]=[CH2:3]

참가 물질

5

실험 절차

327a (390 mg, 1 mmol) and N,O-dimethylhydroxylamine (148 mg, 1.52 mmol) were stirred at −20° C. in anhydrous THF, while Isopropylmagnesium chloride in THF (2M, 1.65 mL, 3.23 mmol) were slowly added. The reaction mixture was allowed to warm to r.t. during 30′, followed by an additional stirring at r.t. for 30′. The reaction is quenched with ammoniumchloride solution (20%). The aqueous layer is extracted with t-butylmethylether, and the combined organic layers are washed with brine, dried over MgSO4 and evaporated to dryness. The crude is purified by flash chromatography on silica gel using cyclohexan/EtOAc 1:1 as eluent. 327b (380 mg, 90%) was obtained as a colourless solid: H1 NMR (DMSO d6) δ7.53 (d, J=3.7 Hz, 1H), 7.16 (d, J=3.6 1H), 5.89 (m, 2H), 5.24 (m, 4H), 3.86 (s, 2H), 3.62 (m, 5H), 3.15 (m, 7H), 2.74 (m, 1H), 2.50 (m, 2H), 2.25 (m, 2H), 1.84 (m, 2H), 1.63 (m, 2H). M/Z APCI: 428.1 (M+1).

후처리

  1. additionwere slowly added
  2. customThe reaction is quenched with ammoniumchloride solution (20%)
  3. extractionThe aqueous layer is extracted with t-butylmethylether
  4. washthe combined organic layers are washed with brine
  5. dry with materialdried over MgSO4
  6. customevaporated to dryness
  7. customThe crude is purified by flash chromatography on silica gel

출처 및 근거

ORD 기록
ord-2eb64060d63f40a8aa28df90d6cb0309
출처 데이터셋
uspto-grants-2011_09
특허 번호
US08012995B1

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