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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107775Generated: October 31, 2026

4-Fluorobenzylamine → HCID 54365091, compound

https://huagongshe.com/reaction/1107775

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzylamineHCID 67326—
Reactant1-(2-Butenyl)-7-chloro-2,3-dimethylpyrrolo[2,3-d]pyridazineHCID 53719624—
ProductHCID 54365091HCID 54365091—

Reaction Conditions

Temperature180 °C

Reaction Steps

A solution of 0.35 g (0.0015 mole) of 1-(2-butenyl)-7-choro-2,3-dimethylpyrrolo[2,3-d]pyridazine dissolved in 3.5 ml of 4-fluorobenzylamine was heated at 180° C. for 2.5 hours. After completion of the reaction, the reaction mixture was allowed to cool to room temperature and then poured into ice-water. The aqueous mixture was extracted with dichloromethane. The extract was dried over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by column chromatography through silica gel using a 30:1 mixture of chloroform and methanol as an eluent to give 0.22 g of 1-(2-butenyl)-7-(4-fluorobenzylamino)-2,3-dimethylpyrrolo[2,3-d]pyridazine (cis/trans=1/4) as a flesh-colored powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06063782
Source datasetuspto-grants-2000_05
ORD IDord-c1905e71c266401599719cb63c886cb2
Source noteuspto-grants-2000_05