反応式
[Cl:1][C:2]1[C:8]([N+:9]([O-:11])=[O:10])=[CH:7][C:5]([NH2:6])=[C:4]([CH3:12])[CH:3]=1.C(C1C=CC([N+]([O-])=O)=CC=1N[S:25]([CH3:28])(=[O:27])=[O:26])C>>[Cl:1][C:2]1[C:8]([N+:9]([O-:11])=[O:10])=[CH:7][C:5]([NH:6][S:25]([CH3:28])(=[O:27])=[O:26])=[C:4]([CH3:12])[CH:3]=1参加物
3
実験手順
Intermediate 79A was prepared from 4-chloro-2-methyl-5-nitroaniline following the procedure employed in the preparation of Intermediate 78A. HPLC: Rt=1.618 min. (CHROMOLITH® column 4.6×50 mm eluting with 10-90% aqueous methanol over 4 min. containing 0.1% TFA, 4 mL/min., monitoring at 220 nm). MS (ES): m/z=265 [M+H]+.
後処理
- washHPLC: Rt=1.618 min. (CHROMOLITH® column 4.6×50 mm eluting with 10-90% aqueous methanol over 4 min. containing 0.1% TFA, 4 mL/min., monitoring at 220 nm)
出典と根拠
- ORDレコード
- ord-ff5e1cd0c2a5486fa1bb29d77912bb22
- 出典データセット
- uspto-grants-2012_08
- 特許番号
- US08252795B2
関連ノート
読み込み中…