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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927115Generated: October 31, 2026

Triethylamine → HCID 71270194, compound

https://huagongshe.com/reaction/927115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(5,6-Bis(benzyloxy)pyridazin-3-yl)(cyclopropyl)methanolHCID 71270347—
SolventDichloromethaneHCID 6344—
ProductHCID 71270194HCID 7127019456%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

(5,6-bis(Benzyloxy)pyridazin-3-yl)(cyclopropyl)methanol (Intermediate 64, 0.34 g, 0.94 mmol) was dissolved in dichloromethane (10.2 ml) and cooled at 0-5° C. under nitrogen atmosphere. Triethylamine (0.474 g, 4.70 mmol) and methanesulfonylchloride (0.162 g, 1.401 mmol) were added to the reaction and it was allowed to stir at room temperature for 3 hours. Upon completion the reaction was quenched by pouring into saturated aqueous sodium bicarbonate solution (25 ml) and the product was extracted into ethyl acetate (2×50 ml). The combined organics were separated, washed with brine, dried (Na2SO4) and concentrated in vacuo. The crude compound was purified by column chromatography (silica, 0-10% ethyl acetate in n-hexane) to afford 3,4-bis(benzyloxy)-6-(cyclopropylidenemethyl)pyridazine (0.18 g, 56% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290456B2
Source datasetuspto-grants-2016_03
ORD IDord-483dd7fb19174e1eb5c509b955999b12
Source noteuspto-grants-2016_03