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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734529Generated: October 31, 2026

Benzyl Alcohol → 1-Benzyl-7-benzyloxy-2-methylpyrrolo[2,3-d]pyridazine

https://huagongshe.com/reaction/1734529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
Reactant1-Benzyl-7-chloro-2-methylpyrrolo[2,3-d]pyridazineHCID 19437748—
ReactantPotassium tert-butoxideHCID 23665647—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1-Benzyl-7-benzyloxy-2-methylpyrrolo[2,3-d]pyridazineHCID 1943774068%

Reaction Steps

650 mg (6 mmol) of benzyl alcohol, 10 ml of N-methylpyrrolidone, 1.1 g (10 mmol) of potassium tert-butoxide, 50 mg (0.2 retool) of [18]crown-6 and 500 mg (1.94 retool) of 1-benzyl-7-chloro-2-methylpyrrolo[2,3-d]pyridazine are reacted at room temperature for 2 h. Purification: chromatography on silica gel (eluent: toluene/dioxane=2:1) and crystallization from diisopropyl ether. Yield: 68%, m.p.: 124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534515
Source datasetuspto-grants-1996_07
ORD IDord-ff2bbf0a58004ffba39a3770036cd0eb
Source noteuspto-grants-1996_07