Ethyl 2-(2-aminothiazol-5-ylthio)acetate → HCID 57668318, compound

HRID 1363783Notes

Reaction equation

HRID 1363783 reaction equation
C([O:3][C:4](=[O:34])[CH2:5][S:6][C:7]1[S:11][C:10]([NH:12][C:13]([N:15]([CH2:28][CH:29]2[CH2:33][CH2:32][CH2:31][CH2:30]2)[C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([C:22](=[O:27])[NH:23][CH:24]([CH3:26])[CH3:25])[CH:17]=2)=[O:14])=[N:9][CH:8]=1)C.C1(CN(C2C=CC(S(C)(=O)=O)=CC=2)C(=O)NC2SC=C(CC(O)=O)N=2)CCCC1.C1(CCNC2C=C(C=CC=2)C(NC(C)C)=O)CCCC1.C(OC(=O)CSC1SC(N)=NC=1)C>>[CH:29]1([CH2:28][N:15]([C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([C:22](=[O:27])[NH:23][CH:24]([CH3:25])[CH3:26])[CH:17]=2)[C:13](=[O:14])[NH:12][C:10]2[S:11][C:7]([S:6][CH2:5][C:4]([OH:34])=[O:3])=[CH:8][N:9]=2)[CH2:33][CH2:32][CH2:31][CH2:30]1

Participants

5

Reactant 4

HCID 21455623Ethyl 2-(2-aminothiazol-5-ylthio)acetateHCID 57668194{2-[3-Cyclopentylmethyl-3-(4-methanesulfonyl-phenyl)-ureido]thiazol-4-yl}-acetic acidHCID 66961963HCID 66961963, compoundHCID 86629916HCID 86629916, compound

Product 1

HCID 57668318HCID 57668318, compound

Procedure

The title compound was prepared via {2-[3-cyclopentylmethyl-3-(3-isopropylcarbamoyl-phenyl)-ureido]-thiazol-5-ylsulfanyl}-acetic acid ethyl ester in a similar manner as described for the synthesis of {2-[3-cyclopentylmethyl-3-(4-methanesulfonyl-phenyl)-ureido]-thiazol-4-yl}-acetic acid, using 3-(cyclopentylethyl-amino)-N-isopropyl-benzamide and (2-amino-thiazol-5-ylsulfanyl)acetic acid ethyl ester.

Sources & evidence

ORD record
ord-6d7cd8561ceb4b2b85cdff1ff5c5ced7
Source dataset
uspto-grants-2011_02
Patent number
US07884210B2

Reaction notes

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