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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215015Generated: October 30, 2026

Methanesulfonyl chloride → HCID 10228158, compound

https://huagongshe.com/reaction/2215015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 10223346HCID 10223346—
SolventDichloromethaneHCID 6344—
ProductHCID 10228158HCID 1022815812.6%

Reaction Steps

A mixture of 5-methyl-1-phenyl-2-phenylamino-7-piperazin-1-yl-1H-[1,8]naphthyridin-4-one (22.6 mg, 0.055 mmol) and MsCl (0.083 mmol, 0.006 mL) in CH2Cl2 (0.8 mL) was stirred at room temperature overnight at which time the solvent was removed in vacuo. The resulting residue was purified by prep-TLC to give 7-(4-methanesulfonyl-piperazin-1-yl)-5-methyl-1-phenyl-2-phenylamino-1H-[1,8]naphthyridin-4-one (3.4 mg, 6%): LCMS RT: 2.36 min, MH+: 490.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109196B2
Source datasetuspto-grants-2006_09
ORD IDord-8f0286e4e68f49f4a3c2ff82c6db4035
Source noteuspto-grants-2006_09