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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067574Generated: November 1, 2026

Diisopropylethylamine → N-[6-[3-[4-(diphenylmethoxy)piperidino]propylamino]-3-methylimidazo[1,2-b]pyridazine-2-carbonyl]glycine ethyl ester

https://huagongshe.com/reaction/1067574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(Diphenylmethoxy)-1-piperidinepropaneamineHCID 10969393—
ReactantN-(6-chloro-3-methylimidazo[1,2-b]pyridazine-2-carbonyl)glycine ethyl esterHCID 22989322—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductN-[6-[3-[4-(diphenylmethoxy)piperidino]propylamino]-3-methylimidazo[1,2-b]pyridazine-2-carbonyl]glycine ethyl esterHCID 2298921435.8%

Reaction Conditions

Temperature95 °C

Reaction Steps

1.17 g of 4-(diphenylmethoxy)-1-piperidinepropanamine and 0.891 g of N-(6-chloro-3-methylimidazo[1,2-b]pyridazine-2-carbonyl)glycine ethyl ester were dissolved in 10 ml of 1-methyl-2-pyrrolidone; 0.517 ml of N-ethyldiisopropylamine was added, followed by stirring in an oil bath (90-100° C.) for 15 hours. After cooling, ice water was added, followed by extraction with ethyl acetate; the extract was washed with saline and dried with magnesium sulfate. The dry product was concentrated under reduced pressure; the residue was subjected to silica gel column chromatography and eluted with ethyl acetate:methanol:triethylamine (90:10:1). The desired fraction was collected and recrystallized with ethyl acetate-ethyl ether (1:1) to yield 0.629 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248740B1
Source datasetuspto-grants-2001_06
ORD IDord-e5b0148dadfd4b1399aa5c505198964e
Source noteuspto-grants-2001_06