Methoxymethyl-triphenylphosphonium chloride → 5-bromo-3-[1-(2-ethyl-2H-pyrazol-3-yl)-2-methoxy-vinyl]-pyridin-2-ylamine

HRID 2234667노트

반응식

HRID 2234667 반응식
[Cl-].[CH3:2][O:3][CH2:4][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C[Si]([N-][Si](C)(C)C)(C)C.[K+].[NH2:34][C:35]1[C:40]([C:41]([C:43]2[N:44]([CH2:48][CH3:49])[N:45]=[CH:46][CH:47]=2)=O)=[CH:39][C:38]([Br:50])=[CH:37][N:36]=1>O1CCCC1>[Br:50][C:38]1[CH:39]=[C:40]([C:41]([C:43]2[N:44]([CH2:48][CH3:49])[N:45]=[CH:46][CH:47]=2)=[CH:2][O:3][CH3:4])[C:35]([NH2:34])=[N:36][CH:37]=1

참가 물질

5

실험 절차

To a solution of (methoxymethyl)triphenylphosphonium chloride (866 mg, 2.53 mmol) in tetrahydrofuran (20 ml) was added potassium bis(trimethylsilyl)amide (5.0 ml, 0.5M, 2.5 mmol). The red-orange reaction mixture was stirred at room temperature for 45 minutes. A solution of (2-amino-5-bromo-pyridin-3-yl)-(2-ethyl-2H-pyrazol-3-yl)-methanone (339 mg, 1.15 mmol) in tetrahydrofuran (10 ml) was added to the reaction mixture. The combined solution was stirred for 4 hours, and then quenched with saturated, aqueous ammonium chloride. The mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over sodium sulfate, and concentrated in vacuo. The crude material was purified by flash chromatography (0 to 100% [10% methanol in ethyl acetate] in hexanes) to give 280 mg (75%) of 5-bromo-3-[1-(2-ethyl-2H-pyrazol-3-yl)-2-methoxy-vinyl]-pyridin-2-ylamine. MS: m/z 323.2+325.2 (M+H+).

후처리

  1. stirringThe combined solution was stirred for 4 hours
  2. customquenched with saturated, aqueous ammonium chloride
  3. extractionThe mixture was extracted with ethyl acetate
  4. washThe organic layer was washed with water
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated in vacuo
  7. customThe crude material was purified by flash chromatography (0 to 100% [10% methanol in ethyl acetate] in hexanes)

출처 및 근거

ORD 기록
ord-2715ec34cbe74aa99444226c91fd53dc
출처 데이터셋
uspto-grants-2010_05
특허 번호
US07709645B2

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