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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036655Generated: October 29, 2026

Aminopyridazine → (1-Imidazo[1,2-b]pyridazin-2-yl-ethyl)-carbamic acid benzyl ester

https://huagongshe.com/reaction/2036655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAminopyridazineHCID 230373—
ReactantBenzyl (4-bromo-3-oxobutan-2-yl)carbamateHCID 73196234—
SolventEthanolHCID 702—
Product(1-Imidazo[1,2-b]pyridazin-2-yl-ethyl)-carbamic acid benzyl esterHCID 67433032—

Reaction Steps

A mixture of pyridazin-3-ylamine (2 g, 21.05 mmol) and (3-bromo-1-methyl-2-oxopropyl)-carbamic acid benzyl ester (7.5 g, 25.26 mmol) in EtOH (25 mL) was heated to reflux overnight. After completion, the reaction mixture was cooled to rt. EtOH was removed in vacuo. The residue was dissolved in EtOAc. The organic layer was dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by column chromatography using silica gel (100-200 mesh) and 0-5% MeOH in DCM to provide (1-imidazo[1,2-b]pyridazin-2-yl-ethyl)-carbamic acid benzyl ester: LC-MS (ESI) m/z 297.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575183B2
Source datasetuspto-grants-2013_11
ORD IDord-39e76ec047ac4006adff339bc5247f70
Source noteuspto-grants-2013_11