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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250606Generated: October 31, 2026

HCID 68803838, compound → HCID 68802898, compound

https://huagongshe.com/reaction/2250606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68803838HCID 68803838—
ReactantHCID 178418546HCID 178418546—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 68802898HCID 6880289860%

Reaction Conditions

Temperature170 °C

Reaction Steps

A mixture of ethyl 5-[4-(5-bromo-3-pyridinyl)-7-ethyl-2-methylpyrrolo[1,2-b]pyridazin-3-yl]pentanoate (167 mg) and copper(I) cyanide (37 mg) in 1-methyl-2-pyrrolidinone (3 mL) was stirred at 170° C. for 4 hours. The mixture was partitioned between ethyl acetate and water. The organic layer was separated, washed with water and brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was purified by silica gel column chromatography eluting with a mixture of hexane and ethyl acetate (20:1-5:1) to give ethyl 5-[4-(5-cyano-3-pyridinyl)-7-ethyl-2-methylpyrrolo[1,2-b]pyridazin-3-yl]pentanoate as an yellow oil (88 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317009B2
Source datasetuspto-grants-2008_01
ORD IDord-9a8c564efa7243288a637402e195d1fb
Source noteuspto-grants-2008_01