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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47232Generated: October 25, 2026

Triphosgene → 6-chloro-7-(morpholin-4-yl)-2H-1,2,4-triazolo[4,3-b]pyridazin-3-one

https://huagongshe.com/reaction/47232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphosgeneHCID 94429—
Reactant6-Chloro-5-(morpholin-4-yl)pyridazin-3-ylhydrazineHCID 216108—
Solvent1,2-DichloroethaneHCID 11—
Product6-chloro-7-(morpholin-4-yl)-2H-1,2,4-triazolo[4,3-b]pyridazin-3-oneHCID 22744168172.1%

Reaction Steps

Triphosgene (750 mg, 2.5 mmol) was added to a stirred solution of 6-chloro-5-(morpholin-4-yl)pyridazin-3-ylhydrazine (1.42 g, 6.2 mmol) in 1,2-dichloroethane (60 ml) at room temperature under nitrogen. The mixture was then stirred and heated at reflux for 22 hours. Upon cooling the precipitate was collected by filtration. The solid was washed with diethyl ether and then dried in vacuo to give 6-chloro-7-(morpholin-4-yl)-2H-1,2,4-triazolo[4,3-b]pyridazin-3-one (1.1 g, 67%) which was used without further purification. Data for the title compound: 1H NMR (250 MHz, d6-DMSO) δ3.02-3.05 (4H, m), 3.72-3.76 (4H, m), 7.19 (1H, s), 12.57 (1H, br s); MS (ES+) m/e 256, 258 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699859B1
Source datasetuspto-grants-2004_03
ORD IDord-9a5030848b034b208688aef850c24c30
Source noteuspto-grants-2004_03