HCID 2758314, compound → HCID 178460756, compound

HRID 1881080Notes

Reaction equation

HRID 1881080 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH2:10][CH2:11][N:12]([C@H:28]2[CH2:33][CH2:32][C@H:31]([CH3:34])[CH2:30][CH2:29]2)[C:13](=[O:27])[NH:14][C:15]2[S:16][C:17]([S:20][C:21]([CH3:26])([CH3:25])[C:22]([OH:24])=[O:23])=[CH:18][N:19]=2)[CH:5]=[CH:6][C:7]=1OC.OCCC1C=C([F:44])C=C(F)C=1.C(OC(=O)C(SC1SC(N)=NC=1)(C)C)C>>[F:44][C:6]1[CH:5]=[C:4]([CH2:10][CH2:11][N:12]([C@H:28]2[CH2:29][CH2:30][C@H:31]([CH3:34])[CH2:32][CH2:33]2)[C:13](=[O:27])[NH:14][C:15]2[S:16][C:17]([S:20][C:21]([CH3:26])([CH3:25])[C:22]([OH:24])=[O:23])=[CH:18][N:19]=2)[CH:3]=[C:2]([F:1])[CH:7]=1

Participants

4

Reactant 3

HCID 2758314HCID 2758314, compoundHCID 57481427Ethyl 2-[(2-amino-1,3-thiazol-5-yl)sulfanyl]-2-methylpropanoateHCID 178490373HCID 178490373, compound

Product 1

HCID 178460756HCID 178460756, compound

Procedure

The compound was prepared following an analogous procedure to the one described for the synthesis of 2-{2-[3-[2-(3-fluoro-4-methoxy-phenyl)-ethyl]-3-(trans-4-methyl -cyclohexyl)-ureido]-thiazol-5-ylsulfanyl}-2-methyl-propionic acid using 1-(2-hydroxy-ethyl) -3,5-difluoro-benzene and 2-(2-amino-thiazol-5-ylsulfanyl)-2-methyl-propionic acid ethyl ester.

Workup

  1. customThe compound was prepared

Sources & evidence

ORD record
ord-9a1b68d3c2c34ba5bfbf6869b5a79c77
Source dataset
uspto-grants-2012_11
Patent number
US08318778B2

Reaction notes

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