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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263801Generated: November 1, 2026

Triethylamine → 4-[3-[5-(4-Ethanesulfonyl-piperazin-1-ylmethyl)-thiazol-2-yl]-1-(4-methyl-cyclohexyl)-ureido]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2263801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-[3-(5-Formyl-thiazol-2-yl)-1-(4-methyl-cyclohexyl)-ureido]-piperidine-1-carboxylic acid tert-butyl esterHCID 57883803—
ReactantPiperazine ethane sulfonamide hydrochlorideHCID 86611202—
Product4-[3-[5-(4-Ethanesulfonyl-piperazin-1-ylmethyl)-thiazol-2-yl]-1-(4-methyl-cyclohexyl)-ureido]-piperidine-1-carboxylic acid tert-butyl esterHCID 5788381558%

Reaction Steps

Prepared as described in general procedure (P) using 4-[3-(5-formyl-thiazol-2-yl)-1-(4-methyl-cyclohexyl)-ureido]-piperidine-1-carboxylic acid tert-butyl ester (200 mg, 0.45 mmol), piperazine ethane sulfonamide hydrochloride (125 mg, 0.58 mmol), triethyl amine (80 μL, 0.58 mmol) and sodium triacetoxyborohydride (113 mg, 0.53 mmol) to afford 160 mg (58%) of the desired product after purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851636B2
Source datasetuspto-grants-2010_12
ORD IDord-d2e6df00ce0e4c4fa7ccd438ad7d26da
Source noteuspto-grants-2010_12