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Methyl 6-(3-(benzyloxy)-2,6-difluorophenyl)-5-fluoropicolinate → HCID 59226549, 화합물

HRID 1523518
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HRID 1523518 반응식
C([O:8][C:9]1[C:10]([F:27])=[C:11]([C:16]2[N:21]=[C:20]([C:22]([O:24][CH3:25])=[O:23])[CH:19]=[CH:18][C:17]=2[F:26])[C:12]([F:15])=[CH:13][CH:14]=1)C1C=CC=CC=1>CO.C(OCC)(=O)C.[Pd]>[F:27][C:10]1[C:9]([OH:8])=[CH:14][CH:13]=[C:12]([F:15])[C:11]=1[C:16]1[N:21]=[C:20]([C:22]([O:24][CH3:25])=[O:23])[CH:19]=[CH:18][C:17]=1[F:26]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 59226393Methyl 6-(3-(benzyloxy)-2,6-difluorophenyl)-5-fluoropicolinate

생성물 1

HCID 59226549HCID 59226549, 화합물수율 86%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 887Methanol용매HCID 8857Ethyl Acetate용매

실험 절차

To a solution of methyl 6-(3-(benzyloxy)-2,6-difluorophenyl)-5-fluoropicolinate (1.0 equiv.) in methanol (0.1 M) was added 10% Pd/C (0.1 equiv.) in ethyl acetate. The reaction was placed under an atmosphere of hydrogen and stirred for 2 hours. Upon completion, the solution was filtered over a pad of Celite, the pad was washed with methanol, the filtrate was concentrated in vacuo to give methyl 6-(2,6-difluoro-3-hydroxyphenyl)-5-fluoropicolinate as a grey oil in 86% yield. LC/MS=284.0 (M+H), Rt=0.90 min.

후처리

  1. filtrationUpon completion, the solution was filtered over a pad of Celite
  2. washthe pad was washed with methanol
  3. concentrationthe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-88e02eeab29c4d3f88956d15f478dea5
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09079889B2

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