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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840282Generated: October 31, 2026

Triethylamine → HCID 23447721, compound

https://huagongshe.com/reaction/1840282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 15518516HCID 15518516—
ReactantEthyl acetate hexaneHCID 21226206—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23447721HCID 2344772152.9%

Reaction Steps

Triethylamine (278.7 mg) and ethyl chlorocarbonate (298.9 mg) were added under ice cooling to a solution of 5,6-bis(4-methoxyphenyl)-4-carboxy-2-isobutyl-2H-pyridazin-3-one (750 mg, 1.84 mmol) in tetrahydrofuran (8 ml), followed by stirring for 1 hour. The reaction mixture was filtered. Under ice cooling, sodium borohydride (277.8 mg) was added to the filtrate, followed by stirring for 1 hour. The mixture was stirred further at room temperature for 2 hours. The reaction mixture was concentrated, to which a saturated aqueous solution of ammonium chloride was added. After the mixture was extracted with ethyl acetate, the extract was washed with a saturated aqueous solution of sodium hydrogencarbonate and water, successively, and was the dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The residue was separated and purified by chromatography on a silica gel column and then crystallized from ethyl acetate-hexane, whereby the title compound (383.0 mg, yield: 52.9%) was obtained as colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06680316B1
Source datasetuspto-grants-2004_01
ORD IDord-1b7512a68f8d49b3a27a828594195e7c
Source noteuspto-grants-2004_01