Ethyl 2-(2-aminothiazol-5-ylthio)acetate → HCID 67050172, compound

HRID 2044000Notes

Reaction equation

HRID 2044000 reaction equation
C([O:3][C:4](=[O:30])[CH2:5][S:6][C:7]1[S:11][C:10]([NH:12][C:13]([N:15]([C:22]2[CH:27]=[CH:26][CH:25]=[C:24]([CH3:28])[C:23]=2[F:29])CC2CCCC2)=[O:14])=[N:9][CH:8]=1)C.[CH:31]1(CN(C2C=CC(S(C)(=O)=O)=CC=2)C(=O)NC2SC=C(CC(O)=O)N=2)[CH2:35][CH2:34][CH2:33][CH2:32]1.[CH:60]1(CNC2C=CC=C(C)C=2F)CCCC1.C(OC(=O)CSC1SC(N)=NC=1)C>>[CH:31]1([N:15]([C:22]2[CH:27]=[CH:26][CH:25]=[C:24]([CH3:28])[C:23]=2[F:29])[C:13](=[O:14])[N:12]([CH3:60])[C:10]2[S:11][C:7]([S:6][CH2:5][C:4]([OH:3])=[O:30])=[CH:8][N:9]=2)[CH2:35][CH2:34][CH2:33][CH2:32]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 66961026N-(Cyclopentylmethyl)-2-fluoro-3-methylanilineHCID 86629948HCID 86629948, compound

Product 1

HCID 67050172HCID 67050172, compound

Procedure

The title compound was prepared via {2-[3-(2-fluoro-3-methyl-phenyl)-3-cyclopentylmethyl-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 cyclopentylmethyl-(2-fluoro-3-methyl-phenyl)amine and (2-amino-thiazol-5-ylsulfanyl)acetic acid ethyl ester

Sources & evidence

ORD record
ord-7fdc3754a369438b87002e1daf24b7ee
Source dataset
uspto-grants-2013_11
Patent number
US08586614B2

Reaction notes

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