Hydrochloric Acid → 1-[3-Mercapto-2-(methoxycarbonylmethyl)propanoyl]-L-proline
Reaction equation
C([S:4][CH2:5][CH:6]([CH2:17][C:18]([O:20][CH3:21])=[O:19])[C:7]([N:9]1[CH2:16][CH2:15][CH2:14][C@H:10]1[C:11]([OH:13])=[O:12])=[O:8])(=O)C.Cl.[Cl-].[Na+]>O.N>[SH:4][CH2:5][CH:6]([CH2:17][C:18]([O:20][CH3:21])=[O:19])[C:7]([N:9]1[CH2:16][CH2:15][CH2:14][C@H:10]1[C:11]([OH:13])=[O:12])=[O:8]Participants
6
Procedure
2.1 g. of the product from Example 81 is dissolved in a mixture of water (35 ml.) and concentrated ammonia (35 ml.) under a blanket of argon. After 20 minutes, the solution is chilled in an ice bath, made acidic with concentrated hydrochloric acid, saturated with sodium chloride and extracted with ethyl acetate. The organic layer is dried and concentrated to dryness in vacuo to yield 1.1 g. of the named product that is purified by chromatography on silica gel (benzene:acetic acid 75:25) Rf : 0.35 (silica gel-benzene:acetic acid, 75:25).
Workup
- temperaturethe solution is chilled in an ice bath
- extractionextracted with ethyl acetate
- customThe organic layer is dried
- concentrationconcentrated to dryness in vacuo
- customto yield 1.1 g
- customof the named product that is purified by chromatography on silica gel (benzene:acetic acid 75:25) Rf
Sources & evidence
- ORD record
- ord-b2d5c3185364422eb7af20dd621a986b
- Source dataset
- uspto-grants-1987_09
- Patent number
- US04690936
Reaction notes
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