1-Methylcyclobutan-1-amine hydrochloride → 8-Bromo-3-cyclopropyl-7-fluoro-2-((1-methylcyclobutyl)amino)quinazolin-4(3H)-one
反応式
[Br:1][C:2]1[C:3]([F:21])=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([NH:12][C:13]1([CH3:16])[CH2:15][CH2:14]1)[N:8]([CH:17]1[CH2:19][CH2:18]1)[C:7]2=[O:20].Br[C:23]1C(F)=CC=C2C=1N=C(Cl)N(C1CC1)C2=O.Cl.CC1(N)CCC1>>[Br:1][C:2]1[C:3]([F:21])=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([NH:12][C:13]1([CH3:16])[CH2:14][CH2:15][CH2:23]1)[N:8]([CH:17]1[CH2:18][CH2:19]1)[C:7]2=[O:20]参加物
4
反応物 3
生成物 1
実験手順
8-Bromo-3-cyclopropyl-7-fluoro-2-((1-methylcyclobutyl)amino)quinazolin-4(3H)-one (498a) was prepared according to the procedures described for Intermediate 495a, using 8-bromo-2-chloro-3-cyclopropyl-7-fluoroquinazolin-4(3H)-one (721) and 1-methylcyclobutanamine hydrochloride (Oakwood Chemical) as the starting materials. MS (ESI, pos. ion) m/z: 366.0/368.0 (M+1).