HCID 11726468, compound → HCID 10325489, compound

HRID 2255334Notes

Reaction equation

HRID 2255334 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8][CH2:9][CH2:10][CH2:11][C:12]([O:14]CC)=[O:13].[CH:17]([N:30]1[C:38]2[C:33](=[CH:34][C:35](/[C:39](/[CH3:44])=[CH:40]/[C:41](O)=[O:42])=[CH:36][CH:37]=2)[CH:32]=[CH:31]1)([C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>>[CH:17]([N:30]1[C:38]2[C:33](=[CH:34][C:35](/[C:39](/[CH3:44])=[CH:40]/[C:41]([NH:1][C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=3[S:8][CH2:9][CH2:10][CH2:11][C:12]([OH:14])=[O:13])=[O:42])=[CH:36][CH:37]=2)[CH:32]=[CH:31]1)([C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1)[C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1

Participants

3

Reactant 2

HCID 11726468HCID 11726468, compoundHCID 14695053HCID 14695053, compound

Product 1

HCID 10325489HCID 10325489, compound

Procedure

0.37 g of amorphous compound 51 was obtained in a similar manner to those described in the Examples 1 and 2 using 1.30 g of ethyl 4-(2-aminophenylthio)butyrate and 1.0 g of 3-(1-benzhydrylindol-5-yl)isocrotonic acid obtained according to the procedures described in the Reference Examples 1-4.

Workup

  1. customobtained

Sources & evidence

ORD record
ord-ce72bac3dd4a4e76a778ad3a2bd8afd1
Source dataset
uspto-grants-1993_08
Patent number
US05239083

Reaction notes

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