Cyclopropylamine → Ethyl 4'-(2-cyclopropylaminobutoxy)-3'-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate
反応式
Cl[CH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([C:13]2[CH:18]=[CH:17][C:16]([C:19]([O:21][CH2:22][CH3:23])=[O:20])=[CH:15][CH:14]=2)=[CH:9][C:8]=1[C:24]1[CH:33]=[CH:32][C:31]2[C:30]([CH3:35])([CH3:34])[CH2:29][CH2:28][C:27]([CH3:37])([CH3:36])[C:26]=2[CH:25]=1.[CH:38]1([NH2:41])[CH2:40][CH2:39]1>C(O)C>[CH:38]1([NH:41][CH:4]([CH2:3][CH3:2])[CH2:5][O:6][C:7]2[CH:12]=[CH:11][C:10]([C:13]3[CH:18]=[CH:17][C:16]([C:19]([O:21][CH2:22][CH3:23])=[O:20])=[CH:15][CH:14]=3)=[CH:9][C:8]=2[C:24]2[CH:33]=[CH:32][C:31]3[C:30]([CH3:35])([CH3:34])[CH2:29][CH2:28][C:27]([CH3:37])([CH3:36])[C:26]=3[CH:25]=2)[CH2:40][CH2:39]1参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
In a manner similar to that of Example 1c, by reaction of 700 mg (1.3 mmol) of ethyl 4′-(4-chlorobutoxy)-3′-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate with 800 μl (11.5 mmol) of cyclopropylamine in 100 ml of ethanol. 180 mg of ethyl 4′-(2-cyclopropylaminobutoxy)-3′-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)biphenyl-4-carboxylate are obtained in the form of a yellow oil (yield=26%).
出典と根拠
- ORDレコード
- ord-dd8be8b7a55744f0bab5445712b9bbf6
- 出典データセット
- uspto-grants-2011_01
- 特許番号
- US07872026B2
反応ノート
読み込み中…