2-Chloro-4-hydrazinylpyridine hydrochloride → 5-(3-Methoxy-5-trifluoromethoxyphenyl)-1-(2-chloropyridin-4-yl)-1H-pyrazole-3-carboxylic acid

HRID 930034노트

반응식

HRID 930034 반응식
[Li].[CH3:2][O:3][C:4]1[CH:5]=[C:6]([C:15]([O-])=[CH:16][C:17](=O)[C:18]([O:20]CC)=[O:19])[CH:7]=[C:8]([O:10][C:11]([F:14])([F:13])[F:12])[CH:9]=1.ClC1C=C(C2N(C3C=CC=CN=3)N=C(C(O)=O)C=2)C=C(F)C=1.Cl.[Cl:48][C:49]1[CH:54]=[C:53]([NH:55][NH2:56])[CH:52]=[CH:51][N:50]=1>>[CH3:2][O:3][C:4]1[CH:5]=[C:6]([C:15]2[N:55]([C:53]3[CH:52]=[CH:51][N:50]=[C:49]([Cl:48])[CH:54]=3)[N:56]=[C:17]([C:18]([OH:20])=[O:19])[CH:16]=2)[CH:7]=[C:8]([O:10][C:11]([F:12])([F:13])[F:14])[CH:9]=1

참가 물질

4

실험 절차

500 mg (1.29 mmol) of the compound of Example 10A is reacted analogously to the synthesis of the compound of Example 20A with 256 mg (1.42 mmol) of 2-chloropyridin-4-yl-hydrazine hydrochloride. After hydrolysis, 149 mg (28% of theory) of the title compound is obtained.

출처 및 근거

ORD 기록
ord-df32efde80f3458ab37210f2ee7857d4
출처 데이터셋
uspto-grants-2016_03
특허 번호
US09296720B2

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