HCID 1953544, compound → HCID 24812389, compound

HRID 1361535Notes

Reaction equation

HRID 1361535 reaction equation
[Cl:1][C:2]1[CH:27]=[CH:26][CH:25]=[CH:24][C:3]=1[CH2:4][O:5][C:6]1[CH:7]=[C:8]([CH:12]=[C:13]([O:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=2[Cl:23])[CH:14]=1)[C:9](O)=[O:10].[CH2:28]([O:30][C:31](=[O:40])[CH2:32][S:33][C:34]1[S:38][C:37]([NH2:39])=[N:36][CH:35]=1)[CH3:29]>>[CH2:28]([O:30][C:31](=[O:40])[CH2:32][S:33][C:34]1[S:38][C:37]([NH:39][C:9](=[O:10])[C:8]2[CH:12]=[C:13]([O:15][CH2:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[Cl:23])[CH:14]=[C:6]([O:5][CH2:4][C:3]3[CH:24]=[CH:25][CH:26]=[CH:27][C:2]=3[Cl:1])[CH:7]=2)=[N:36][CH:35]=1)[CH3:29]

Participants

3

Reactant 2

HCID 1953544HCID 1953544, compoundHCID 21455623Ethyl 2-(2-aminothiazol-5-ylthio)acetate

Product 1

HCID 24812389HCID 24812389, compound

Procedure

The title compound was prepared from 3,5-bis-(2-chloro-benzyloxy)-benzoic acid and (2-amino-thiazol-5-ylsulfanyl)-acetic acid ethyl ester following general procedure A.

Sources & evidence

ORD record
ord-d3b6618dc12140e5ab4392ac9f4b6f49
Source dataset
uspto-grants-2011_02
Patent number
US07880012B2

Reaction notes

Loading…