4-Bromo-3-methylthiophenecarboxylic acid → 4-Bromo-N-(5-(cyclopropylcarbamoyl)-2-methylphenyl)-3-methylthiophene-2-carboxamide
反応式
[Br:1][C:2]1[C:3]([CH3:10])=[C:4]([C:7]([OH:9])=O)[S:5][CH:6]=1.Cl.[NH2:12][C:13]1[CH:14]=[C:15]([CH:22]=[CH:23][C:24]=1[CH3:25])[C:16]([NH:18][CH:19]1[CH2:21][CH2:20]1)=[O:17]>>[Br:1][C:2]1[C:3]([CH3:10])=[C:4]([C:7]([NH:12][C:13]2[CH:14]=[C:15]([C:16](=[O:17])[NH:18][CH:19]3[CH2:21][CH2:20]3)[CH:22]=[CH:23][C:24]=2[CH3:25])=[O:9])[S:5][CH:6]=1参加物
3
実験手順
The compound a was prepared by coupling commercially available 4-bromo-3-methylthiophene-2-carboxylic acid with 3-amino-N-cyclopropyl-4-methylbenzamide hydrochloride (prepared as described in WO 04/071440) using the method described in Example 128. HPLC Ret time=3.12 min. LCMS [M+H]+ 393.13.
後処理
- customThe compound a was prepared
- customHPLC Ret time=3.12 min
出典と根拠
- ORDレコード
- ord-080b5d3829454cc69072f9a44d8f5b8e
- 出典データセット
- uspto-grants-2013_03
- 特許番号
- US08404689B2
反応ノート
読み込み中…