Sodium borohydride → HCID 68183395、化合物
反応式
[NH2:1][C:2]1[C:3]([C:12]([C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([F:20])[CH:15]=2)=O)=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[CH:9][CH:8]=[CH:7]2.[CH3:21][NH:22][S:23](Cl)(=[O:25])=[O:24].[BH4-].[Na+]>N1C=CC=CC=1>[F:20][C:16]1[CH:15]=[C:14]([CH:12]2[C:3]3[CH:4]=[CH:5][C:6]4[C:11](=[N:10][CH:9]=[CH:8][CH:7]=4)[C:2]=3[NH:1][S:23](=[O:25])(=[O:24])[N:22]2[CH3:21])[CH:19]=[CH:18][CH:17]=1参加物
5
実験手順
In a similar fashion using route 27 general procedure 70, (8-amino-quinolin-7-yl)-(3-fluoro-phenyl)-methanone (Intermediate 374) (100 mg, 0.38 mmol), N-methylsulfamoyl chloride (Intermediate 213) (146 mg, 1.13 mmol) and NaBH4 (14 mg, 0.38 mmol) in pyridine (3 ml) gave the title compound (50 mg, 39%) after purification by preparative HPLC (acidic conditions 1).