Methyl 2-(3-chloro-5-nitrophenyl)-3,3-dimethyl-1,2,3,4-tetrahydroquinoline-6-carboxylate → Methyl 2-(3-amino-5-chlorophenyl)-3,3-dimethyl-1,2,3,4-tetrahydroquinoline-6-carboxylate
反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:11]2[C:20]([CH3:22])([CH3:21])[CH2:19][C:18]3[C:13](=[CH:14][CH:15]=[C:16]([C:23]([O:25][CH3:26])=[O:24])[CH:17]=3)[NH:12]2)[CH:5]=[C:6]([N+:8]([O-])=O)[CH:7]=1>C(O)C.O.Cl.[Fe]>[NH2:8][C:6]1[CH:5]=[C:4]([CH:11]2[C:20]([CH3:21])([CH3:22])[CH2:19][C:18]3[C:13](=[CH:14][CH:15]=[C:16]([C:23]([O:25][CH3:26])=[O:24])[CH:17]=3)[NH:12]2)[CH:3]=[C:2]([Cl:1])[CH:7]=1参加物
5
反応物 1
生成物 1
試薬・触媒・溶媒 3
実験手順
To a solution of methyl 2-(3-chloro-5-nitrophenyl)-3,3-dimethyl-1,2,3,4-tetrahydroquinoline-6-carboxylate (124 mg, 0.33 mmol) in ethanol/water (2 mL/0.5 mL) was added 2 drops of conc. hydrochloric acid and iron (370 mg, 6.62 mmol). The mixture was stirred and heated to reflux for 4 h. LC-MS showed most of SM was consumed. The mixture was dried over silica gel and washed through a short column with petroleum ether:ethyl acetate=3:1 to afford 95 mg of methyl 2-(3-amino-5-chlorophenyl)-3,3-dimethyl-1,2,3,4-tetrahydroquinoline-6-carboxylate as a brown solid. (Yield=83%). MS (ESI+APCI) M+1=345.
後処理
- temperatureheated
- temperatureto reflux for 4 h
- customwas consumed
- customThe mixture was dried over silica gel
- washwashed through a short column with petroleum ether
出典と根拠
- ORDレコード
- ord-7474e2e21fd74ce8ada07e9b9519f99b
- 出典データセット
- uspto-grants-2013_11
- 特許番号
- US08586747B2
反応ノート
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