Hydrochloric Acid → 1-[3-Mercapto-2-(methoxycarbonylmethyl)propanoyl]-L-proline

HRID 2049782Notes

Reaction equation

HRID 2049782 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

1-[3-(Acetylthio)-2-(methoxycarbonylmethyl)propanoyl]-L-proline (2.1 g.) is dissolved in a mixture of water (35 ml.) and concentrated ammonia (35 ml.) under a blanket of argon. After twenty 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 1-[3-mercapto-2-(methoxycarbonylmethyl)propanoyl]-L-proline that is purified by chromatography on silica gel (benzene:acetic acid 75:25). Rf : 0.35 (silica gel, benzene:acetic acid, 75:25).

Workup

  1. waitAfter twenty minutes
  2. temperaturethe solution is chilled in an ice bath
  3. extractionextracted with ethyl acetate
  4. customThe organic layer is dried
  5. concentrationconcentrated to dryness in vacuo
  6. customto yield 1.1 g
  7. customof 1-[3-mercapto-2-(methoxycarbonylmethyl)propanoyl]-L-proline that is purified by chromatography on silica gel (benzene:acetic acid 75:25)

Sources & evidence

ORD record
ord-b69d7a0572d24c64b7140e7fc3c2c645
Source dataset
uspto-grants-1980_04
Patent number
US04198517

Reaction notes

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