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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620374Generated: October 29, 2026

Dimethylformamide → HCID 21246144, compound

https://huagongshe.com/reaction/620374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium HydroxideHCID 14798—
ReactantEpibromohydrinHCID 18430—
ReactantSodium hydrideHCID 24758—
ReactantBenzofuro[2,3-c]pyridazineHCID 21246139—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 21246144HCID 21246144—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a stirred solution of benzofuro[2,3-c]pyridazine (5.09 g) in dimethylformamide (40 ml) containing a suspension of sodium hydride (1.68 g, 50% oil) was added dry methanol (1.5 ml). The mixture was heated to 70° C. for 30 minutes and treated with epibromohydrin (10.2 ml) and stirring was continued at room temperature for 150 minutes. The mixture was poured into water (300 ml), taken to pH 10 with sodium hydroxide, extracted into dichloromethane and the organic extract was evaporated under reduced pressure to afford an oil that was purified by column chromatography (silica, chloroformpetrol, chloroform, chloroform-methanol) to afford 4-[2-(2,3-epoxypropoxy)phenyl]-3-methoxypyridazine as an oil. This was heated under reflux for 60 minutes with t-butylamine (20 ml) in methanol (50 ml) and the mixture was allowed to stand overnight. Evaporation under reduced pressure afford an oil which on treat ment with diethyl ether-petrol gave 4-(2-[3-t-butylamino-2-hydroxypropoxy)phenyl]-3-methoxypyridazine, m.p. 109.5°-110.5° C. from cyclohexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04820819
Source datasetuspto-grants-1989_04
ORD IDord-985592f93122492990d7d1d373a4d00a
Source noteuspto-grants-1989_04