2-Amino-4-methylthiazole → HCID 16117448、化合物
反応式
Cl[C:2]1[C:11]2[N:10]=[C:9]([CH3:12])[CH:8]=[CH:7][C:6]=2[C:5](B(O)O)=[CH:4][N:3]=1.I[C:17]1[CH:22]=[N:21][CH:20]=[C:19]([C:23]([F:26])([F:25])[F:24])[N:18]=1.[NH2:27][C:28]1[S:29][CH:30]=[C:31]([CH3:33])[N:32]=1>>[CH3:33][C:31]1[N:32]=[C:28]([NH:27][C:2]2[N:3]=[CH:4][C:5]([C:17]3[CH:22]=[N:21][CH:20]=[C:19]([C:23]([F:26])([F:25])[F:24])[N:18]=3)=[C:6]3[C:11]=2[N:10]=[C:9]([CH3:12])[CH:8]=[CH:7]3)[S:29][CH:30]=1参加物
4
実験手順
The title compound, MS: m/e=403.3 (M+H+), was prepared in accordance with the general method of example 15 step 1 and step 3 from 8-chloro-2-methyl-[1,7]naphthyridine-5-boronic acid (Example L), 2-iodo-6-trifluoromethyl-pyrazine (Example O) and 2-amino-4-methylthiazole.
出典と根拠
- ORDレコード
- ord-1bdcfb67bcbc4b75ae2faabb8da8f78a
- 出典データセット
- uspto-grants-2009_03
- 特許番号
- US07511055B2
反応ノート
読み込み中…