1,4-Dioxane hydrochloride → HCID 70074454, compound
Reaction equation
[CH2:1]([O:8][C:9](=[O:40])[C@H:10]([CH:37]([CH3:39])[CH3:38])[NH:11][C:12](=[O:36])[C@@H:13]([CH2:32][CH:33]([CH3:35])[CH3:34])[NH:14][C:15](=[O:31])[CH:16]([OH:30])[CH:17]1[CH2:22][CH2:21][CH2:20][CH2:19][N:18]1C(OC(C)(C)C)=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[ClH:41].O1CCOCC1>ClCCl>[ClH:41].[CH2:1]([O:8][C:9](=[O:40])[C@H:10]([CH:37]([CH3:39])[CH3:38])[NH:11][C:12](=[O:36])[C@@H:13]([CH2:32][CH:33]([CH3:34])[CH3:35])[NH:14][C:15](=[O:31])[CH:16]([OH:30])[CH:17]1[CH2:22][CH2:21][CH2:20][CH2:19][NH:18]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
[2-Hydroxy-2-(N-t-butyloxycarbonylpiperidin-2-yl)acetyl]-D-leucylvaline benzyl ester (85 mg) was dissolved in dichloromethane (1 ml) and a 4N hydrochloric acid/dioxane solution (1 ml) was added to the solution under cooling with ice to conduct a reaction at room temperature for 2 h. The reaction liquid was concentrated under reduced pressure and the residue was washed with n-hexane several times and dried to give [2-hydroxy-2-(piperidin-2-yl)acetyl]-D-leucylvaline benzyl ester hydrochloride.
Workup
- temperatureunder cooling with ice
- customa reaction at room temperature for 2 h
- customThe reaction liquid
- concentrationwas concentrated under reduced pressure
- washthe residue was washed with n-hexane several times
- customdried
Sources & evidence
- ORD record
- ord-6c8af84295c2481fb239de8df384d5ec
- Source dataset
- uspto-grants-1993_06
- Patent number
- US05221752
Reaction notes
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