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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655606Generated: November 2, 2026

Sodium Hydroxide → HCID 178457029, compound

https://huagongshe.com/reaction/1655606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 19792029HCID 19792029—
SolventMethanolHCID 887—
ProductHCID 178457029HCID 178457029—

Reaction Steps

Ethyl 6-trifluoromethylpyridin-2-one-3-carboxylate, prepared by the method described in Helv. Chim. Acta. 71, 596 (1988), is chlorinated with phosphorus oxychloride to give the 2-chloro compound. Treatment of ethyl 2-chloro-6-trifluoromethylpyridine-3-carboxylate with N-triphenylmethyl-5-[2-(4'-propylaminomethyl-biphenyl)]tetrazole, prepared as described in Example 72B, in tetrahydrofuran containing triethylamine affords the tertiary amine. Treatment of ethyl 2-{N-propyl-N-[(2'-[N-triphenylmethyl-1H-tetrazol-5-yl]biphenyl-4-yl)methyl]amino}-6-trifluoromethyl-pyridine-3-carboxylate with p-toluenesulfonic acid monohydrate in methanol to detritylate followed by sodium hydroxide in methanol hydrolysis gives the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250548
Source datasetuspto-grants-1993_10
ORD IDord-5df91f4412ba475c95388e818eacf4bf
Source noteuspto-grants-1993_10