Hydrochloric Acid → 1-(2-Methyl-3-sulfanylpropanoyl)-L-proline
Reaction equation
O1CCCCC1[S:7][CH2:8][CH:9]([CH3:20])[C:10]([N:12]1[CH2:19][CH2:18][CH2:17][C@H:13]1[C:14]([OH:16])=[O:15])=[O:11].Cl>CO>[SH:7][CH2:8][CH:9]([CH3:20])[C:10]([N:12]1[CH2:19][CH2:18][CH2:17][C@H:13]1[C:14]([OH:16])=[O:15])=[O:11]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 1-[3-(tetrahydropyran-2-ylthio)-2-methylpropanoyl)-L-proline (1 g.) in a mixture of methanol (25 ml.) and concentrated hydrochloric acid (25 ml.) is stored at room temperature for 30 minutes. The solvents are removed in vacuo to yield 1-(3-mercapto-2-methylpropanoyl)-L-proline. Rf : 0.35 (silica gel, Benzene/acetic acid, 3:1), Rf 0.5 (silica gel, Methyl-ethylketone/acetic acid/pyridine/water (14:1:2:1) identical to the compound of Example 34.
Workup
- customThe solvents are removed in vacuo
Sources & evidence
- ORD record
- ord-39e867d6ef6c43e992303f43ce4414e9
- Source dataset
- uspto-grants-1979_05
- Patent number
- US04154840
Reaction notes
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