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Trifluoroacetic acid → 1-(4-{3-[(1S)-2-Methoxy-1-methylethoxy]-5-[5-(1,3-thiazol-2-yl)-1H-pyrrol-2-yl]phenoxy}phenyl)ethanone

HRID 1964568
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HRID 1964568 반응식
[C:1]([C:4]1[CH:39]=[CH:38][C:7]([O:8][C:9]2[CH:10]=[C:11]([C:21]3[N:22](C(OC(C)(C)C)=O)[C:23]([C:26]4[S:27][CH:28]=[CH:29][N:30]=4)=[CH:24][CH:25]=3)[CH:12]=[C:13]([O:15][C@@H:16]([CH3:20])[CH2:17][O:18][CH3:19])[CH:14]=2)=[CH:6][CH:5]=1)(=[O:3])[CH3:2].FC(F)(F)C(O)=O>ClCCl>[CH3:19][O:18][CH2:17][C@H:16]([CH3:20])[O:15][C:13]1[CH:14]=[C:9]([CH:10]=[C:11]([C:21]2[NH:22][C:23]([C:26]3[S:27][CH:28]=[CH:29][N:30]=3)=[CH:24][CH:25]=2)[CH:12]=1)[O:8][C:7]1[CH:38]=[CH:39][C:4]([C:1](=[O:3])[CH3:2])=[CH:5][CH:6]=1
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반응물 2

HCID 6422Trifluoroacetic acidHCID 66683501t-Butyl 2-{3-(4-acetylphenoxy)-5-[(1S)-2-methoxy-1-methylethoxy]phenyl}-5-(1,3-thiazol-2-yl)-1H-pyrrole-1-carboxylate

생성물 1

HCID 580654701-(4-{3-[(1S)-2-Methoxy-1-methylethoxy]-5-[5-(1,3-thiazol-2-yl)-1H-pyrrol-2-yl]phenoxy}phenyl)ethanone수율 94%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

t-Butyl 2-{3-(4-acetylphenoxy)-5-[(1S)-2-methoxy-1-methylethoxy]phenyl}-5-(1,3-thiazol-2-yl)-1H-pyrrole-1-carboxylate (73 mg, 0.133 mmol) synthesized in Example (39a) was dissolved in dichloromethane (1.0 mL). Trifluoroacetic acid (2.0 mL) was added dropwise with stirring under nitrogen atmosphere, and stirring was carried out at room temperature for 2.5 hours. The solvent was distilled off under reduced pressure, and the resulting residue was purified using silica gel column chromatography (elution solvent: ethyl acetate/hexane=30%-40%) to afford the desired compound (56 mg, yield 94%) as a pale yellow liquid.

후처리

  1. stirringstirring
  2. distillationThe solvent was distilled off under reduced pressure
  3. customthe resulting residue was purified
  4. washsilica gel column chromatography (elution solvent: ethyl acetate/hexane=30%-40%)

출처 및 근거

ORD 기록
ord-52fb425bb48a48c2abfaaf484c94d03a
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08415359B2

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