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Trifluoroacetic acid → 1-(3-methoxybutan-2-yl)-2-methyl-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid

HRID 1527082
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반응식

HRID 1527082 반응식
[CH3:1][O:2][CH:3]([CH3:23])[CH:4]([N:6]1[C:10]2=[N:11][CH:12]=[CH:13][CH:14]=[C:9]2[C:8]([C:15]([O:17]C(C)(C)C)=[O:16])=[C:7]1[CH3:22])[CH3:5].FC(F)(F)C(O)=O>C(Cl)Cl>[CH3:1][O:2][CH:3]([CH3:23])[CH:4]([N:6]1[C:10]2=[N:11][CH:12]=[CH:13][CH:14]=[C:9]2[C:8]([C:15]([OH:17])=[O:16])=[C:7]1[CH3:22])[CH3:5]
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참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 89740318tert-butyl 1-(3-methoxybutan-2-yl)-2-methyl-1H-pyrrolo[2,3-b]pyridine-3-carboxylate

생성물 1

HCID 1177786071-(3-methoxybutan-2-yl)-2-methyl-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
27 °C

실험 절차

To the pre-cooled solution of tert-butyl 1-(3-methoxybutan-2-yl)-2-methyl-1H-pyrrolo[2,3-b]pyridine-3-carboxylate (3.0 g, 9.42 mmol) in CH2Cl2 (20 mL) was added trifluoroacetic acid (20 mL) dropwise. The solution was stirred at 27° C. for 1.5 hours. The solvent was removed under vacuum at 27° C. The residue was used for next step without purified. LCMS (M+H+) m/z: calcd 263.30. found 262.9.

후처리

  1. customThe solvent was removed under vacuum at 27° C
  2. customwithout purified

출처 및 근거

ORD 기록
ord-88b151a5c50d4f99b617d7ba0038bdef
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09085583B2

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