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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718627Generated: October 30, 2026

tert-Butyl 4-(2-(hydroxymethyl)-8-morpholinoimidazo[1,2-b]pyridazin-3-yl)-5,6-dihydropyridine-1(2H)-carboxylate → tert-Butyl 4-(2-(hydroxymethyl)-8-morpholinoimidazo[1,2-b]pyridazin-3-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/718627

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(2-(hydroxymethyl)-8-morpholinoimidazo[1,2-b]pyridazin-3-yl)-5,6-dihydropyridine-1(2H)-carboxylateHCID 117733826—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-Butyl 4-(2-(hydroxymethyl)-8-morpholinoimidazo[1,2-b]pyridazin-3-yl)piperidine-1-carboxylateHCID 117733827—

Reaction Steps

To a solution of compound 41a (3.5 g, 8.4 mmol) in methanol (30 mL) was added 10% Pd/C (ca. 50% water, 3.5 g). The resulting mixture was hydrogenated at about 2 to 3 atm overnight, and filtered through a pad of diatomaceous earth. The filtrate was concentrated under reduced pressure to obtain compound 41b as a white solid. Mass Spectrum (LCMS, ESI pos.): Calcd. for C21H31N5O4: 418.2 (M+H). found: 418.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193736B2
Source datasetuspto-grants-2015_11
ORD IDord-0ebba9e8fb21485bb6d5065c452ad4f7
Source noteuspto-grants-2015_11