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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015643Generated: October 29, 2026

Methanol → HCID 16074975, compound

https://huagongshe.com/reaction/1015643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantHCID 67299243HCID 67299243—
SolventAcetic AcidHCID 176—
SolventMethanol tetrahydrofuran waterHCID 21892291—
ProductHCID 16074975HCID 1607497585%

Reaction Conditions

Temperature55 °C

Reaction Steps

4-{[(2,4-Dichloro-benzoyl)-(2-methoxycarbonyl-5-phenyl-thiophen-3-yl)-amino]-methyl}-piperidine-1-carboxylic acid benzyl ester (150 mg, 0.24 mmol) was dissolved in a mixture of THF:MeOH:H2O (3:2:1, 2.4 mL) and treated with LiOH.H2O (29.6 mg, 0.7 mmol). The solution was heated at 55° C. for 2 h. The solvents were removed and the residue was acidified using HCl. The product was extracted with EtOAc and the organic layers were washed with brine and dried. The residue was purified by silica gel column chromatography using EtOAc:MeOH:AcOH as eluent to provide 4-{[(2-Carboxy-5-phenyl-thiophen-3-yl)-(2,4-dichloro-benzoyl)-amino]-methyl}-piperidine-1-carboxylic acid benzyl ester (124 mg, 85% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985769B2
Source datasetuspto-grants-2011_07
ORD IDord-07366594f6ac4eeea21343982c38f730
Source noteuspto-grants-2011_07