Hydrochloric Acid → HCID 20037736, compound
Reaction equation
C([O:3][C:4](=[O:20])[CH2:5][N:6]([C:12](=[O:19])[CH:13]([CH3:18])[CH2:14][S:15][CH2:16][CH3:17])[CH:7]1[CH2:11][CH2:10][CH2:9][CH2:8]1)C.Cl>[OH-].[Na+]>[CH2:16]([S:15][CH2:14][CH:13]([CH3:18])[C:12]([N:6]([CH:7]1[CH2:11][CH2:10][CH2:9][CH2:8]1)[CH2:5][C:4]([OH:20])=[O:3])=[O:19])[CH3:17]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 3.8 g (0.012) of N-(3-ethylthio-2-methyl propanoyl)-N-cyclopentyl glycine ethyl ester in 80 ml of 10% NaOH was stirred for 7 hours. It was then cooled, acidified with 10% HCl, extracted with ether, dried over MgSO4, and evaporated to dryness giving oily residue which was purified by HPLC using HOAc-EtOAc-Hexane (5:45:50).
Workup
- temperatureIt was then cooled
- extractionextracted with ether
- dry with materialdried over MgSO4
- customevaporated to dryness
- customgiving oily residue which
- customwas purified by HPLC
Sources & evidence
- ORD record
- ord-154ea921631046e68c258a585f7e5079
- Source dataset
- uspto-grants-1989_06
- Patent number
- US04839367
Reaction notes
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