反応式
[F:1][C:2]([C:5]1[N:9]([C:10]2[CH:11]=[C:12]([CH:16]=[C:17]([C:19]3[CH:24]=[CH:23][C:22]([CH3:25])=[CH:21][N:20]=3)[CH:18]=2)[C:13](O)=[O:14])[N:8]=[N:7][N:6]=1)([F:4])[CH3:3].[NH2:26][C@H:27]([CH3:30])[CH2:28][OH:29]>>[F:1][C:2]([C:5]1[N:9]([C:10]2[CH:11]=[C:12]([CH:16]=[C:17]([C:19]3[CH:24]=[CH:23][C:22]([CH3:25])=[CH:21][N:20]=3)[CH:18]=2)[C:13]([NH:26][C@@H:27]([CH3:30])[CH2:28][OH:29])=[O:14])[N:8]=[N:7][N:6]=1)([F:4])[CH3:3]参加物
3
実験手順
3-[5-(1,1-Difluoro-ethyl)-tetrazol-1-yl]-5-(5-methyl-pyridin-2-yl)-benzoic acid was reacted with (R)-2-amino-propan-1-ol using the procedure of step 4 of Example 5, to afford 3-[5-(1,1-Difluoro-ethyl)-tetrazol-1-yl]-N—((S)-2-hydroxy-1-methyl-ethyl)-5-(5-methyl-pyridin-2-yl)-benzamide, MS (M+H)=403.
出典と根拠
- ORDレコード
- ord-cc407aaea75d4f48b2da7be838e5f90f
- 出典データセット
- uspto-grants-2012_06
- 特許番号
- US08193368B2
関連ノート
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