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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195669Generated: November 1, 2026

Oxalyl chloride → HCID 15166371, compound

https://huagongshe.com/reaction/1195669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2,1,3-Benzoxadiazole-5-carboxylic acidHCID 2735454—
Reactant4-(Aminomethyl)-1-(2-pyridylethyl)piperidineHCID 15166360—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 15166371HCID 1516637140%

Reaction Steps

To a suspension of benzofurazan-5-carboxylic acid (150 mg, 0.91 mmol) in methylene chloride (3.3 ml) was added dimethylformamide (1 drop) followed by dropwise addition of oxalyl chloride (89 μl, 1.0 mmol). The resulting solution was stirred at room temperature for 3 hours and then concentrated under reduced pressure. The brown oil was redissolved in methylene chloride (3.3 ml) and was added to a cooled (0° C.) solution of 4-(aminomethyl)-1-(2-pyridylethyl)piperidine (0.21 g, 0.95 mmol) in methylene chloride (1.6 ml). The reaction mixture was stirred at 0° C. for 11/2 hours. Solvent evaporation, flash chromatography (silica gel, chloroform-methanol-ammonium hydroxide, 95/5/1/2) and trituration with hexane-ethyl acetate gave 4-[N-(benzofurazan-5-carbonyl)aminomethyl]-1-(2-pyridylethyl)piperidine (133 mg, 40%);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112824
Source datasetuspto-grants-1992_05
ORD IDord-7c34f8a7349e4d56b7d3c669edb415c7
Source noteuspto-grants-1992_05