HCID 15837669, compound → HCID 15837672, compound

HRID 1599385Notes

Reaction equation

HRID 1599385 reaction equation
[C:1]([S:4][CH:5]([CH2:9][C:10]1[CH:15]=[CH:14][C:13]([O:16][CH3:17])=[CH:12][CH:11]=1)[C:6]([OH:8])=O)(=[O:3])[CH3:2].[CH3:18][O:19][C:20](=[O:37])[C@@H:21]1[CH2:25][CH2:24][CH:23]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=2[OH:32])[N:22]1[C:33](=[O:36])[CH2:34][NH2:35]>CCCCCC.C(OCC)(=O)C>[CH3:18][O:19][C:20](=[O:37])[C@@H:21]1[CH2:25][CH2:24][CH:23]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=2[OH:32])[N:22]1[C:33](=[O:36])[CH2:34][NH:35][C:6](=[O:8])[CH:5]([S:4][C:1](=[O:3])[CH3:2])[CH2:9][C:10]1[CH:15]=[CH:14][C:13]([O:16][CH3:17])=[CH:12][CH:11]=1

Participants

4

Procedure

Condensation of 2-acetylthio-3-(para-methoxyphenyl)propanoic acid with N-glycyl-5-(ortho-hydroxyphenyl)proline methyl ester, obtained in accordance with the same protocols as those described in Preparation G, yields the expected product in the form of an oil after chromatography in an n-hexane/ethyl acetate mixture, 4:6.

Workup

  1. customobtained in accordance with the same protocols as
  2. customthose described in Preparation G

Sources & evidence

ORD record
ord-0ac94415f54b497d8cd65a271cfbe18c
Source dataset
uspto-grants-1998_04
Patent number
US05741781

Reaction notes

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