2-(Bromomethyl)-1,3-dichloro-5-methoxybenzene → 1-[4-(tert-Butyl-dimethyl-silanyloxy)-cyclohexyl]-3-(2,6-dichloro-4-methoxy-benzyl)-pyrrolidin-2-one

HRID 2235302노트

반응식

HRID 2235302 반응식
[C:1]([Si:5]([CH3:20])([CH3:19])[O:6][C@@H:7]1[CH2:12][CH2:11][C@H:10]([N:13]2[CH2:17][CH2:16][CH2:15][C:14]2=[O:18])[CH2:9][CH2:8]1)([CH3:4])([CH3:3])[CH3:2].Br[CH2:22][C:23]1[C:28]([Cl:29])=[CH:27][C:26]([O:30][CH3:31])=[CH:25][C:24]=1[Cl:32]>>[C:1]([Si:5]([CH3:20])([CH3:19])[O:6][CH:7]1[CH2:8][CH2:9][CH:10]([N:13]2[CH2:17][CH2:16][CH:15]([CH2:22][C:23]3[C:24]([Cl:32])=[CH:25][C:26]([O:30][CH3:31])=[CH:27][C:28]=3[Cl:29])[C:14]2=[O:18])[CH2:11][CH2:12]1)([CH3:4])([CH3:3])[CH3:2]

참가 물질

3

실험 절차

Using the procedure to synthesize Example 202 and using the reagents of cis-1-[4-(tert-butyl-dimethyl-silanoxy)-cyclohexyl]-pyrrolidin-2-one (Preparation 17) and 2-Bromomethyl-1,3-dichloro-5-methoxy-benzene (Preparation 62). Warm reaction to room temperature, quench with NH4Cl (sat), dilute with diethyl ether, wash with brine, dry over sodium sulfate, filter and evaporate to an oil. Chromatography (silica, 100% hexanes to 75:25 hexanes/EtoAc) yields 1-[4-(tert-Butyl-dimethyl-silanyloxy)-cyclohexyl]-3-(2,6-dichloro-4-methoxy-benzyl)-pyrrolidin-2-one in 49% yield. The silylether is dissolved in THF, treated with 10.0 equivalents of HCl (conc) and allowed to stir at room temperature for 3 h, quench reaction with water, dilute with EtOAc, adjust pH to 7.0, separate, dry over sodium sulfate, filter and evaporate provides the titled compound in 84% yield: Mass spectrum (API-ES positive) m/z=372 (M+H).

후처리

  1. customto synthesize Example 202
  2. temperatureWarm
  3. customreaction to room temperature
  4. customquench with NH4Cl (sat)
  5. additiondilute with diethyl ether
  6. washwash with brine
  7. dry with materialdry over sodium sulfate
  8. filtrationfilter
  9. customevaporate to an oil

출처 및 근거

ORD 기록
ord-7725e73ccc5c48c4a97c12fa2697e6b3
출처 데이터셋
uspto-grants-2010_05
특허 번호
US07713979B2

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