Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734523Generated: October 31, 2026

Bromine → 1-Benzyl-3-bromo-7-(4-fluorobenzyloxy)-2-methylpyrrolo[2,3-d]pyridazine

https://huagongshe.com/reaction/1734523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant1-Benzyl-7-(4-fluorobenzyloxy)-2-methylpyrrolo[2,3-d]pyridazineHCID 19437762—
SolventDichloromethaneHCID 6344—
Product1-Benzyl-3-bromo-7-(4-fluorobenzyloxy)-2-methylpyrrolo[2,3-d]pyridazineHCID 1943775979.4%

Reaction Steps

A solution of 180 μl (3.5 mmol) of bromine in 7 ml of anhydrous dichloromethane is added dropwise at 0° C. to a solution of 910 mg (2.6 mmol) of 1-benzyl-7-(4-fluorobenzyloxy)-2-methylpyrrolo[2,3-d]pyridazine in 15 ml of anhydrous dichloromethane in the course of 30 min. The solution is kept at 0° C. for a further 1 h, then treated with 50 ml of ice-water and extracted. The organic phase is separated off, washed with 3×25 ml of water, dried over magnesium sulfate and concentrated. The residue is chromatographed on silica gel (eluent: ethyl acetate). The fractions of Rf=0.6 are concentrated and crystallized from diisopropyl ether/cyclohexane. 880 mg (79%) of the title compound are isolated. M.p.: 128°-130° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534515
Source datasetuspto-grants-1996_07
ORD IDord-6e412ba8c0f94063835bbc09a187d28f
Source noteuspto-grants-1996_07