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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162431Generated: October 29, 2026

Acetic Anhydride → N-(6-chloroimidazo[1,2-b]pyridazin-2-yl)acetamide

https://huagongshe.com/reaction/1162431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant2-Amino-6-chloroimidazo[1,2-b]pyridazineHCID 49758021—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-(6-chloroimidazo[1,2-b]pyridazin-2-yl)acetamideHCID 5951951066.9%

Reaction Steps

To a solution of 6-chloroimidazo[1,2-b]pyridazin-2-amine (18 g, 106.5 mmol) in DCM (180 mL) was added triethylamine (10.8 g, 106.5 mmol), DMAP (1.32 g, 1.06 mmol), and acetic anhydride (6 g, 106.5 mmol) sequentially at rt. The reaction mixture was stirred for 5 h at rt and the precipitate was filtered and washed with 50 mL of methanol to afford the title compound (15 g, 66%). 1H NMR (DMSO-d6, 300 MHz): δ 7.3 (d, 1H), 8.02 (d, 1H), 8.25 (s, 1H). LCMS (M+1) 211 (99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820665B2
Source datasetuspto-grants-2010_10
ORD IDord-174b31240f82450282c5297214fcc8c1
Source noteuspto-grants-2010_10