Cyclopentylmethyl-(4-methanesulfonyl-phenyl)-amine → {2-[3-Cyclopentylmethyl-3-(4-methanesulfonyl-phenyl)-ureido]-thiazole-5-sulfonylamino}-acetic acid

HRID 1363750Notes

Reaction equation

HRID 1363750 reaction equation
C([O:3][C:4](=[O:35])[CH2:5][NH:6][S:7]([C:10]1[S:14][C:13]([NH:15][C:16]([N:18]([CH2:29][CH:30]2[CH2:34][CH2:33][CH2:32][CH2:31]2)[C:19]2[CH:24]=[CH:23][C:22]([S:25]([CH3:28])(=[O:27])=[O:26])=[CH:21][CH:20]=2)=[O:17])=[N:12][CH:11]=1)(=[O:9])=[O:8])C.C1(CN(C2C=CC(S(C)(=O)=O)=CC=2)C(=O)NC2SC=C(CC(O)=O)N=2)CCCC1.C1(CNC2C=CC(S(C)(=O)=O)=CC=2)CCCC1.C(OC(=O)CNS(C1SC(N)=NC=1)(=O)=O)C.COC([C@@H]1CCCN1S(C1SC(N)=NC=1)(=O)=O)=O>>[CH:30]1([CH2:29][N:18]([C:19]2[CH:24]=[CH:23][C:22]([S:25]([CH3:28])(=[O:26])=[O:27])=[CH:21][CH:20]=2)[C:16](=[O:17])[NH:15][C:13]2[S:14][C:10]([S:7]([NH:6][CH2:5][C:4]([OH:35])=[O:3])(=[O:9])=[O:8])=[CH:11][N:12]=2)[CH2:34][CH2:33][CH2:32][CH2:31]1

Participants

6

Reactant 5

HCID 43453307Cyclopentylmethyl-(4-methanesulfonyl-phenyl)-amineHCID 57668194{2-[3-Cyclopentylmethyl-3-(4-methanesulfonyl-phenyl)-ureido]thiazol-4-yl}-acetic acidHCID 86253773(2-Amino-thiazole-5-sulfonylamino)acetic acid ethyl esterHCID 86629877(S)-1-(2-aminothiazole-5-sulfonyl)-pyrrolidine-2-carboxylic acid methyl esterHCID 86629884{2-[3-Cyclopentylmethyl-3-(4-methanesulfonyl-phenyl)ureido]-thiazole-5-sulfonylamino}-acetic acid ethyl ester

Product 1

HCID 57668310{2-[3-Cyclopentylmethyl-3-(4-methanesulfonyl-phenyl)-ureido]-thiazole-5-sulfonylamino}-acetic acid

Procedure

The title compound was prepared via {2-[3-cyclopentylmethyl-3-(4-methanesulfonyl-phenyl)-ureido]-thiazole-5-sulfonylamino}-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 cyclopentylmethyl-(4-methanesulfonyl-phenyl)-amine and (2-amino-thiazole-5-sulfonylamino)-acetic acid ethyl ester the latter prepared in a similar manner as (S)-1-(2-amino-thiazole-5-sulfonyl)-pyrrolidine-2-carboxylic acid methyl ester.

Sources & evidence

ORD record
ord-cc7430725ffd423cbbf9726f340dc805
Source dataset
uspto-grants-2011_02
Patent number
US07884210B2

Reaction notes

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