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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092598Generated: November 1, 2026

1-Butanesulfonyl chloride → HCID 68253359, compound

https://huagongshe.com/reaction/2092598

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Butanesulfonyl chlorideHCID 75430—
ReactantHCID 67329109HCID 67329109—
SolventPyridineHCID 1049—
ProductHCID 68253359HCID 6825335979%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution [6-(5-Amino-2-methyl-phenyl)-5,6,7,8-tetrahydro-pyrido[4,3-d]pyrimidin-2-yl]-[4-(4-methyl-piperazin-1-yl)-phenyl]-amine (50.0 mg, 0.116 mmol) in Pyridine (1 ml) at 0° C. was added Butane-1-sulfonyl chloride (21.3 mg, 0.139 mmol) dropwise The reaction mixture was stirred for 15 minutes at 0° C. and then allowed to attain room temperature. It was then further stirred for 3 hours at room temperature. The reaction mixture was concentrated under vacuum. The reaction mass was then, diluted with water and extracted with dichloromethane. The dichloromethane layer was washed with water, then with brine solution. The organic layer is dried over sodium sulphate and concentrated under reduced pressure. The crude product obtained was purified by column chromatography (SiO2, 2-10% methanol in chloroform) to give 50.4 mg (78.9%) Butane-1-sulfonic acid (4-methyl-3-{2-[4-(4-methyl-piperazin-1-yl)-phenylamino]-7,8-dihydro-5H-pyrido[4,3-d]pyrimidin-6-yl}-phenyl)-amide [49] as off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440679B2
Source datasetuspto-grants-2013_05
ORD IDord-f4c0a9fc4537437d83beb22e1e3d207c
Source noteuspto-grants-2013_05