Hydrochloric Acid → HCID 67020462、化合物
反応式
[C:1]1([CH2:7][CH2:8][N:9]2[CH2:14][CH2:13][CH:12]([C:15]([O:17]CC)=[O:16])[CH2:11][CH2:10]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[ClH:20]>[OH-].[Na+]>[ClH:20].[C:1]1([CH2:7][CH2:8][N:9]2[CH2:14][CH2:13][CH:12]([C:15]([OH:17])=[O:16])[CH2:11][CH2:10]2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1参加物
4
実験手順
A suspension of 1-(2-phenylethyl)-4-carbetoxypiperidine (12.2 g, 0.047 mol) obtained as described in J. Med. Chem. 1996 (39), 749-756, in 1N NaOH (100 ml) was heated under reflux for 4 h. After cooling to room temperature, the solution was made acid with 6N HCl to pH 2, concentrated by evaporation at reduced pressure, and the solid thus obtained was filtered and dried in a stove under vacuum to give the desired product (12.1 g),
後処理
- customobtained
- temperatureunder reflux for 4 h
- concentrationconcentrated by evaporation at reduced pressure
- customthe solid thus obtained
- filtrationwas filtered
- customdried in a stove under vacuum
出典と根拠
- ORDレコード
- ord-d308e8a1450248f09072ba60de7b5939
- 出典データセット
- uspto-grants-2013_04
- 特許番号
- US08415476B2
反応ノート
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