Hydrochloric Acid → (Z)-(S)-[3-(3-methoxy-phenyl)-2-methyl-pent-3-enyl]-dimethyl-amine
反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]([CH2:16][CH3:17])[CH:10]([CH3:15])[CH2:11][N:12]([CH3:14])[CH3:13])[CH:6]=[CH:7][CH:8]=1.Cl>>[CH3:1][O:2][C:3]1[CH:4]=[C:5](/[C:9](=[CH:16]\[CH3:17])/[C@H:10]([CH3:15])[CH2:11][N:12]([CH3:14])[CH3:13])[CH:6]=[CH:7][CH:8]=1参加物
3
実験手順
The yield of [3-(3-methoxy-phenyl)-2-methyl-pentyl]-dimethyl-amine; hydrochloride (3) was >96% with a ratio of the enantiomer (−)-(2R,3R) to the diastereoisomer (−)-(2R,3S) of 76:24. The (−)-(2R,3R) enantiomer is preferably used as an active ingredient in medicaments.
出典と根拠
- ORDレコード
- ord-9e75a225b2f543568d569e62b20eeb79
- 出典データセット
- uspto-grants-2014_04
- 特許番号
- US08704002B2
反応ノート
読み込み中…