Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633499Generated: October 31, 2026

Acetic Anhydride → N-(3-chloro[1,2,4]triazolo[4,3-b]pyridazin-6-yl)acetamide

https://huagongshe.com/reaction/633499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant3-Chloro-[1,2,4]triazolo[4,3-b]pyridazin-6-amineHCID 67524192—
SolventPyridineHCID 1049—
ProductN-(3-chloro[1,2,4]triazolo[4,3-b]pyridazin-6-yl)acetamideHCID 67524510—

Reaction Steps

0.11 cm3 of acetic anhydride is added to a mixture of 202 mg of 3-chloro[1,2,4]triazolo[4,3-b]pyridazin-6-amine in 5 cm3 of pyridine at 0° C. The temperature is allowed to rise to 20° C. over 6 h, then 0.05 cm3 of acetic anhydride is again added and stirring is maintained for 24 h. The precipitate formed is spin-filter-dried and then washed with ethyl ether and pentane. This solid is purified by chromatography on Biotage Quad 12/25 (KP-SIL, 60 A; 32-63 μM), elution being carried out with a gradient of dichloromethane/methanol of 100/0 to 90/10. 41 mg of N-(3-chloro[1,2,4]triazolo[4,3-b]pyridazin-6-yl)acetamide are thus obtained in the form of a white powder, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321777B2
Source datasetuspto-grants-2016_04
ORD IDord-e556d77bad63402a9fad062dfd548f5d
Source noteuspto-grants-2016_04