4-Methylphenethyl alcohol → HCID 178425244, compound

HRID 1810019Notes

Reaction equation

HRID 1810019 reaction equation
F[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.O[CH2:36]CC1C=CC(C)=CC=1.C(OC(=O)C(SC1SC(N)=NC=1)(C)C)C>>[CH3:26][C:21]([S:20][C:17]1[S:16][C:15]([NH:14][C:13]([N:12]([C@H:28]2[CH2:29][CH2:30][C@H:31]([CH3:34])[CH2:32][CH2:33]2)[CH2:11][CH2:10][C:4]2[CH:5]=[CH:6][C:7]([CH3:36])=[CH:2][CH:3]=2)=[O:27])=[N:19][CH:18]=1)([CH3:25])[C:22]([OH:24])=[O:23]

Participants

4

Reactant 3

HCID 952944-Methylphenethyl alcoholHCID 57481427Ethyl 2-[(2-amino-1,3-thiazol-5-yl)sulfanyl]-2-methylpropanoateHCID 178490373HCID 178490373, compound

Product 1

HCID 178425244HCID 178425244, 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)-4-methyl-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-ab3f70cacc5e409e9212abb607d9b893
Source dataset
uspto-grants-2013_01
Patent number
US08362049B2

Reaction notes

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