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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275415Generated: November 2, 2026

Betahistine → HCID 15287677, compound

https://huagongshe.com/reaction/275415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBetahistineHCID 2366—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 9822857HCID 9822857—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15287677HCID 15287677—

Reaction Steps

Oxalyl chloride (0.13 g, 0.00105 moles) was added to a cold (10° C.) solution of trans-[[2-[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]thio]cyclohexyl]thio]acetic acid (0.39 g, 0.00095 mole) in benzene (50 ml). The cold bath was removed and the reaction mixture was stirred at room temperature for 20 hours. The reaction mixture was concentrated in vacuo to an oil. The oil was dissolved in toluene (50 ml) and then concentrated once again. The process was repeated using tetrahydrofuran (25 ml) in place of toluene. To a solution of the oil in tetrahydrofuran (50 ml) was added 2-(2-methylaminoethyl) pyridine (0.13 g, 0.00095 moles) and triethylamine (1 ml) and the reaction mixture was stirred at room temperature for 44 hours. After removal of the while solid precipitate by filtration, the filtrate was concentrated to give the crude product as an oil. The product was purified by silica gel chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05393764
Source datasetuspto-grants-1995_02
ORD IDord-4e403e9a133249848eddc4d86dbbfdde
Source noteuspto-grants-1995_02