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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250626Generated: November 1, 2026

Acetic Anhydride → HCID 69309264, compound

https://huagongshe.com/reaction/2250626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 69311575HCID 69311575—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 69309264HCID 6930926493.6%

Reaction Steps

A mixture of ethyl 5-[2-(aminomethyl)-7-ethyl-4-(5-methyl-3-pyridinyl)pyrrolo[1,2-b]pyridazin-3-yl]pentanoate (67.6 mg) and acetic anhydride (19.2 mg) in dichloromethane (3 mL) was stirred at ambient temperature for 1 hour. The solution was diluted with chloroform, washed with saturated sodium bicarbonate solution and brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was purified by preparative silica gel column chromatography eluting with a mixture of chloroform and methanol (20:1) to give ethyl 5-[2-[(acetylamino)methyl]-7-ethyl-4-(5-methyl-3-pyridinyl)pyrrolo[1,2-b]pyridazin-3-yl]pentanoate as yellow oil (70 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317009B2
Source datasetuspto-grants-2008_01
ORD IDord-0025c1d60eb54b78bc99eec247aaf3d6
Source noteuspto-grants-2008_01