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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734534Generated: October 30, 2026

Acetic Acid → 3-Acetoxymethyl-1-benzyl-7-benzyloxy-2-methylpyrrolo[2,3-d]pyridazine

https://huagongshe.com/reaction/1734534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantSodium BicarbonateHCID 516892—
Reactant1-Benzyl-7-benzyloxy-3-hydroxymethyl-2-methylpyrrolo[2,3-d]pyridazineHCID 19437781—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-Acetoxymethyl-1-benzyl-7-benzyloxy-2-methylpyrrolo[2,3-d]pyridazineHCID 19437760—

Reaction Steps

A solution of 1.65 g (4.59 mmol) of 1-benzyl-7-benzyloxy-3-hydroxymethyl-2-methylpyrrolo [2,3-d]pyridazine, 3.8 g (18.6 mmol) of dicyclohexylcarbodiimide and 1.6 ml (27.4 mmol) of glacial acetic acid in 50 ml of anhydrous tetrahydrofuran is stirred at room temperature for 18 h. The solution is then treated with 50 ml of water, rendered neutral with saturated sodiumhydrogen carbonate solution and extracted with 3×50 ml of dichloromethane. The organic extracts are washed with 50 ml of water, dried over magnesium sulfate and concentrated. The residue which remains is chromatographed on silica gel (eluent: ethyl acetate). After crystallization from diisopropyl ether, 1.3 g (71%) of the title compound are isolated. M.p.: 121°-122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534515
Source datasetuspto-grants-1996_07
ORD IDord-6a45e5ebeb0a4c649b76dfd8b2ba3000
Source noteuspto-grants-1996_07