2,5-Dimethyl-2H-pyrazole-3-carbonyl chloride → N-[4-chloro-5-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)-2-fluorophenyl]-1,3-dimethyl-1H-pyrazole-5-carboxamide

HRID 2391357

反応式

HRID 2391357 の反応式
[NH2:1][C:2]1[C:3]([F:25])=[CH:4][C:5]([Cl:24])=[C:6]([CH:23]=1)[O:7][C:8]1[CH:9]=[CH:10][C:11]2[N:12]([CH:14]=[C:15]([NH:17][C:18]([CH:20]3[CH2:22][CH2:21]3)=[O:19])[N:16]=2)[N:13]=1.[CH3:26][N:27]1[C:31]([C:32](Cl)=[O:33])=[CH:30][C:29]([CH3:35])=[N:28]1>CN(C)C(=O)C>[Cl:24][C:5]1[C:6]([O:7][C:8]2[CH:9]=[CH:10][C:11]3[N:12]([CH:14]=[C:15]([NH:17][C:18]([CH:20]4[CH2:21][CH2:22]4)=[O:19])[N:16]=3)[N:13]=2)=[CH:23][C:2]([NH:1][C:32]([C:31]2[N:27]([CH3:26])[N:28]=[C:29]([CH3:35])[CH:30]=2)=[O:33])=[C:3]([F:25])[CH:4]=1

参加物

4

実験手順

Using N-[6-(5-amino-2-chloro-4-fluorophenoxy)imidazo[1,2-b]pyridazin-2-yl]cyclopropanecarboxamide (200 mg, 0.55 mmol), N,N-dimethylacetamide (4.0 mL) and 1,3-dimethyl-1H-pyrazole-5-carbonyl chloride (105 mg, 0.66 mmol), and in the same manner as in Example 120, the title compound (108 mg, 40%) was obtained as a white powder.

出典と根拠

ORDレコード
ord-43443e07781b45289248858b9cc676d4
出典データセット
uspto-grants-2012_09
特許番号
US08273741B2

関連ノート

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