Hydrochloric Acid → HCID 20037736, compound

HRID 2164783Notes

Reaction equation

HRID 2164783 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

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

  1. temperatureIt was then cooled
  2. extractionextracted with ether
  3. dry with materialdried over MgSO4
  4. customevaporated to dryness
  5. customgiving oily residue which
  6. customwas purified by HPLC

Sources & evidence

ORD record
ord-26a14c271ee5418396a247b8ad614994
Source dataset
uspto-grants-1985_03
Patent number
US04507316

Reaction notes

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