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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047326Generated: October 26, 2026

2-Bromobenzyl alcohol → 2-Bromobenzyl 2-(1-{[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/1047326

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromobenzyl alcoholHCID 72850—
Reactant2-[1-[[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl]-4-piperidinyl]-4-thiazolecarboxylic acidHCID 66601457—
Product2-Bromobenzyl 2-(1-{[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazole-4-carboxylateHCID 66911508—

Reaction Steps

A solution of 2-(1-{[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazole-4-carboxylic acid (III-4, 100 mg) is reacted analogously to Example I-811 with (2-bromophenyl)methanol (49.0 mg). This gives, after chromatographic purification, 2-bromobenzyl 2-(1-{[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazole-4-carboxylate (123 mg, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569509B2
Source datasetuspto-grants-2013_10
ORD IDord-4badac9074a14391b7a190fdd7dc440e
Source noteuspto-grants-2013_10