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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418574Generated: November 3, 2026

Nicotinic Acid → HCID 86751306, compound

https://huagongshe.com/reaction/1418574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNicotinic AcidHCID 938—
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-1-methylpyridinium iodideHCID 167069—
ReactantHCID 86751307HCID 86751307—
SolventDichloromethaneHCID 6344—
ProductHCID 86751306HCID 8675130643%

Reaction Steps

To a stirred mixture of (2R)-4-(3-aminopropyl)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(3,4-dimethylbenzyl)-piperazine dihydrochloride (160 mg), nicotinic acid (33 mg) and triethylamine (0.17 ml) in dichloromethane (2 ml) was added 2-chloro-1-methylpyridinium iodide (78 mg) at room temperature. After stirring for 1.5 hours, the reaction mixture was evaporated under reduced pressure. The residue was partitioned between ethyl acetate (30 ml) and water (10 ml). The organic layer was separated and dried over magnesium sulfate. After evaporation of the solvent, the residue was purified by column chromatography on a silica gel with dichloromethane-methanol (40:1) as eluent to give (2R)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(3,4-dimethylbenzyl)-4-[3-(nicotinoylamino)propyl]-piperazine (70 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883098
Source datasetuspto-grants-1999_03
ORD IDord-bb740deb8cd84990ba775dc405766b10
Source noteuspto-grants-1999_03