Dibenzoyltartaric acid → 3-Methyl-4-piperidyl (3S,4S)-Pivalate
反応式
[CH3:1][C@H:2]1[C@H:7]([O:8][C:9](=[O:14])[C:10]([CH3:13])([CH3:12])[CH3:11])[CH2:6][CH2:5][NH:4][CH2:3]1.C1C=CC(C(O[C@@H](C(O)=O)[C@@H](OC(C2C=CC=CC=2)=O)C(O)=O)=O)=CC=1>CCOC(C)=O>[CH3:1][C@@H:2]1[C@@H:7]([O:8][C:9](=[O:14])[C:10]([CH3:13])([CH3:12])[CH3:11])[CH2:6][CH2:5][NH:4][CH2:3]1参加物
4
実験手順
Racemic 19 (62.7 g, 314.4 mmol) is dissolved in EtOAc (300 ml) and a solution of L-(−)-O,O′-Dibenzoyl tartaric acid (56.3 g, 157.2 mmol) in EtOAc (450 ml) is added. The formed solid is filtered off, washed with cold EtOAc and dried. It is then re-crystallized from hot methanol (400 ml). The crystals are collected and the free base is liberated by treatment with 1N—NaOH and extraction with ether.
後処理
- filtrationThe formed solid is filtered off
- washwashed with cold EtOAc
- customdried
- customIt is then re-crystallized from hot methanol (400 ml)
- customThe crystals are collected
- extractionthe free base is liberated by treatment with 1N—NaOH and extraction with ether
出典と根拠
- ORDレコード
- ord-0978a5f09a774926a4307b02f9b62a0f
- 出典データセット
- uspto-grants-2010_12
- 特許番号
- US07858781B2
反応ノート
読み込み中…