Ethyl 2-(2-aminothiazol-5-ylthio)acetate → HCID 67050188, compound
Reaction equation
C([O:3][C:4](=[O:32])[CH2:5][S:6][C:7]1[S:11][C:10]([NH:12][C:13]([N:15]([C:22]2[CH:23]=[N:24][C:25]([NH:28][C:29](=[O:31])[CH3:30])=[CH:26][CH:27]=2)[CH2:16][CH:17]2C[CH2:20][CH2:19][CH2:18]2)=[O:14])=[N:9][CH:8]=1)C.[CH:33]1(CN(C2C=CC(S(C)(=O)=O)=CC=2)C(=O)NC2SC=C(CC(O)=O)N=2)CCCC1.C1(CNC2C=CC(NC(=O)C)=NC=2)CCCC1.C(OC(=O)CSC1SC(N)=NC=1)C>>[C:29]([NH:28][C:25]1[N:24]=[CH:23][C:22]([N:15]([CH:16]2[CH2:17][CH2:18][CH2:19][CH2:20]2)[C:13](=[O:14])[N:12]([CH3:33])[C:10]2[S:11][C:7]([S:6][CH2:5][C:4]([OH:3])=[O:32])=[CH:8][N:9]=2)=[CH:27][CH:26]=1)(=[O:31])[CH3:30]Participants
5
Reactant 4
Product 1
Procedure
The title compound was prepared via {2-[3-(6-acetylamino-pyridin-3-yl)-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 N-[5-(cyclopentylmethyl-amino)-pyridin-2-yl]-acetamide and (2-amino-thiazol-5-ylsulfanyl)acetic acid ethyl ester
Sources & evidence
- ORD record
- ord-29c615cebc704e5988220be0bfcce1ed
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08586614B2
Reaction notes
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