1-(2-Chloro-4-nitro-benzyl)-pyrrolidine → 3-Chloro-4-pyrrolidin-1-ylmethyl-phenylamine
反応式
[Cl:1][C:2]1[CH:13]=[C:12]([N+:14]([O-])=O)[CH:11]=[CH:10][C:3]=1[CH2:4][N:5]1[CH2:9][CH2:8][CH2:7][CH2:6]1>[Ni].CO>[Cl:1][C:2]1[CH:13]=[C:12]([NH2:14])[CH:11]=[CH:10][C:3]=1[CH2:4][N:5]1[CH2:6][CH2:7][CH2:8][CH2:9]1参加物
4
実験手順
A suspension of 1.00 g (4.155 mmol) 1-(2-chloro-4-nitro-benzyl)-pyrrolidine (140a) and 100 mg Raney nickel in 30 mL MeOH were hydrogenated at RT and 10 psi. The catalyst was filtered off and the filtrate evaporated down i. vac.
後処理
- customwere hydrogenated at RT
- filtrationThe catalyst was filtered off
- customthe filtrate evaporated down i
出典と根拠
- ORDレコード
- ord-4d2e7e4ba93d4199ad52f7f75f41af8e
- 出典データセット
- uspto-grants-2008_04
- 特許番号
- US07351719B2
反応ノート
読み込み中…