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5-Methoxy-6-(trifluoromethyl)indoline → 5-Methoxy-6-trifluoromethyl-1-[4-(pyridin-4-ylthiomethyl)phenyl Carbamoyl]indoline

HRID 1603804
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인쇄 미리보기

반응식

HRID 1603804 반응식
[N:1]1[CH:6]=[CH:5][C:4]([S:7][CH2:8][C:9]2[CH:15]=[CH:14][C:12]([NH2:13])=[CH:11][CH:10]=2)=[CH:3][CH:2]=1.C1(N[C:23](=O)[O-:24])C=CC=CC=1.[CH3:26][O:27][C:28]1[CH:29]=[C:30]2[C:34](=[CH:35][C:36]=1[C:37]([F:40])([F:39])[F:38])[NH:33][CH2:32][CH2:31]2>>[CH3:26][O:27][C:28]1[CH:29]=[C:30]2[C:34](=[CH:35][C:36]=1[C:37]([F:40])([F:38])[F:39])[N:33]([C:23](=[O:24])[NH:13][C:12]1[CH:11]=[CH:10][C:9]([CH2:8][S:7][C:4]3[CH:3]=[CH:2][N:1]=[CH:6][CH:5]=3)=[CH:15][CH:14]=1)[CH2:32][CH2:31]2
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참가 물질

4

반응물 3

HCID 112067135-Methoxy-6-(trifluoromethyl)indolineHCID 18005148Benzenamine, 4-[(4-pyridinylthio)methyl]-HCID 21896570Phenylcarbamate

생성물 1

HCID 180051505-Methoxy-6-trifluoromethyl-1-[4-(pyridin-4-ylthiomethyl)phenyl Carbamoyl]indoline수율 64%

실험 절차

4-(Pyridin-4-ylthiomethyl)aniline (0.37 g, 1.71 mmol) was converted to the phenylcarbamate and treated with 5-methoxy-6-trifluoromethylindoline (D111) (0.37 g, 1.71 mmol) as in the method of Example 26 to give the title compound (0.5 g, 64%) as a white crystalline solid m.p. 174-5° C.

출처 및 근거

ORD 기록
ord-9d08a06f7a7546d8b42c091e0a6c4797
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05990133

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