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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511286Generated: November 2, 2026

Thionyl Chloride → 5-(3-((7-Methoxyquinolin-4-yloxy)methyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)thiophene-2-carbonyl chloride

https://huagongshe.com/reaction/1511286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 67502507HCID 67502507—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product5-(3-((7-Methoxyquinolin-4-yloxy)methyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)thiophene-2-carbonyl chlorideHCID 57691149—

Reaction Steps

To a suspension of 5-(3-((7-methoxyquinolin-4-yloxy)methyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)thiophene-2-carboxylic acid (prepared according to general method A) (0.500 g, 1.15 mmol) in dichloromethane at 0° C. was added thionyl chloride (1.26 ml, 17.3 mmol) dropwise. Three drops DMF were added and the solution was stirred at room temp for three hours. The solution was concentrated to a brown residue and taken forward without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08212041B2
Source datasetuspto-grants-2012_07
ORD IDord-2012370b01d646e191820fc9e413d90b
Source noteuspto-grants-2012_07