Cyclopentanecarbaldehyde → {2-[3-Cyclopentylmethyl-3-(3,4-difluoro-phenyl)-ureido]-thiazole-5-sulfonylamino}-acetic acid

HRID 1363742Notes

Reaction equation

HRID 1363742 reaction equation
C([O:3][C:4](=[O:33])[CH2:5][NH:6][S:7]([C:10]1[S:14][C:13]([NH:15][C:16]([N:18]([CH2:27][CH:28]2[CH2:32][CH2:31][CH2:30][CH2:29]2)[C:19]2[CH:24]=[CH:23][C:22]([F:25])=[C:21]([F:26])[CH:20]=2)=[O:17])=[N:12][CH:11]=1)(=[O:9])=[O:8])C.C1(CN(C2C=CC(F)=C(F)C=2)C(=O)NC2SC=C(CC(O)=O)N=2)CCCC1.FC1C=C(C=CC=1F)N.C1(C=O)CCCC1.C(OC(=O)CNS(C1SC(N)=NC=1)(=O)=O)C.COC([C@@H]1CCCN1S(C1SC(N)=NC=1)(=O)=O)=O>>[CH:28]1([CH2:27][N:18]([C:19]2[CH:24]=[CH:23][C:22]([F:25])=[C:21]([F:26])[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:33])=[O:3])(=[O:8])=[O:9])=[CH:11][N:12]=2)[CH2:32][CH2:31][CH2:30][CH2:29]1

Participants

7

Procedure

The title compound was prepared via {2-[3-cyclopentylmethyl-3-(3,4-difluoro-phenyl)-ureido]-thiazole-5-sulfonylamino}-acetic acid ethyl ester in a similar manner as described for the synthesis of {2-[3-cyclopentylmethyl-3-(3,4-difluoro-phenyl)-ureido]-thiazol-4-yl}-acetic acid, using 3,4-difluoroaniline, cyclopentanecarbaldehyde 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-64ba012d91ff4c2c835603ed52f9e2fe
Source dataset
uspto-grants-2011_02
Patent number
US07884210B2

Reaction notes

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