反応式
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:12][CH2:11][C@H:10]([CH2:13][NH:14][C:15](=[O:21])[O:16][C:17]([CH3:20])([CH3:19])[CH3:18])[CH2:9]2)=[C:4]([F:22])[CH:3]=1.[C:23]1(=O)[CH2:26][CH2:25][CH2:24]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C>>[F:22][C:4]1[CH:3]=[C:2]([NH:1][CH:23]2[CH2:26][CH2:25][CH2:24]2)[CH:7]=[CH:6][C:5]=1[N:8]1[CH2:12][CH2:11][C@H:10]([CH2:13][NH:14][C:15](=[O:21])[O:16][C:17]([CH3:18])([CH3:19])[CH3:20])[CH2:9]1参加物
4
実験手順
tert-Butyl (R)-[1-(4-amino-2-fluorophenyl)pyrrolidin-3-yl]methylcarbamate was alkylated with cyclobutanone using triacetoxyborohydride as reducing agent by method N. This resulted in the product with the molecular weight of 363.48 (C20H30FN3O2); MS (ESI): 364 (M+H+).
後処理
- customThis resulted in the product with the molecular weight of 363.48 (C20H30FN3O2)
出典と根拠
- ORDレコード
- ord-8837c495a450401fa42a2f8e52e75662
- 出典データセット
- uspto-grants-2007_05
- 特許番号
- US07223788B2
関連ノート
読み込み中…