4-(Chloromethyl)benzoyl chloride → 4-chloromethyl-N-(5-cyclohexylamino-[1,2,4]triazolo[1,5-a]pyridin-2-yl)-benzamide
反応式
[CH:1]1([NH:7][C:8]2[N:13]3[N:14]=[C:15]([NH2:17])[N:16]=[C:12]3[CH:11]=[CH:10][CH:9]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[Cl:18][CH2:19][C:20]1[CH:28]=[CH:27][C:23]([C:24](Cl)=[O:25])=[CH:22][CH:21]=1>>[Cl:18][CH2:19][C:20]1[CH:28]=[CH:27][C:23]([C:24]([NH:17][C:15]2[N:16]=[C:12]3[CH:11]=[CH:10][CH:9]=[C:8]([NH:7][CH:1]4[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]4)[N:13]3[N:14]=2)=[O:25])=[CH:22][CH:21]=1参加物
3
実験手順
The title compound was prepared following procedure described for intermediate B1, but starting from N5-cyclohexyl[1,2,4]triazolo[1,5-a]pyridine-2,5-diamine ((A9), 800 mg; 3.46 mmol; 1.0 eq.) and 4-(chloromethyl)benzoyl chloride (981 mg; 5.2 mmol; 1.5 eq.) as a brownish foam (1.32 g, 99%). LC/MS, M+(ESI): 384.0, M−(ESI): 382.0.
出典と根拠
- ORDレコード
- ord-e9046415845342d0a4aa2b117ebfac90
- 出典データセット
- uspto-grants-2012_09