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HCID 67395129, 화합물 → 2-(5-Fluoro-6-phenylpyridin-3-ylamino)-5-methylbenzoic acid

HRID 42058
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반응식

HRID 42058 반응식
[F:1][C:2]1[CH:3]=[C:4]([NH:14][C:15]2[CH:27]=[CH:26][C:25]([CH3:28])=[CH:24][C:16]=2[C:17]([O:19]C(C)(C)C)=[O:18])[CH:5]=[N:6][C:7]=1[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1>C(O)(C(F)(F)F)=O>[F:1][C:2]1[CH:3]=[C:4]([NH:14][C:15]2[CH:27]=[CH:26][C:25]([CH3:28])=[CH:24][C:16]=2[C:17]([OH:19])=[O:18])[CH:5]=[N:6][C:7]=1[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1
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참가 물질

3

반응물 1

HCID 67395129HCID 67395129, 화합물

생성물 1

HCID 251864502-(5-Fluoro-6-phenylpyridin-3-ylamino)-5-methylbenzoic acid

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

A solution of tert-butyl 2-(5-fluoro-6-phenylpyridin-3-ylamino)-5-methylbenzoate (0.83 mmol, 0.313 g) in TFA (5 ml) was stirred at room temperature for 30 minutes. The solvent was reduced under reduced pressure and the crude mixture was purified by reverse phase chromatography using a 30% to 100% (Water-ACN) gradient and affording 0.119 g (40% of yield) of the expected product.

후처리

  1. customthe crude mixture was purified by reverse phase chromatography
  2. customaffording

출처 및 근거

ORD 기록
ord-18a920ce37b24924ac86bc940506d702
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08536165B2

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