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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49306Generated: October 29, 2026

Methanesulfonyl chloride → HCID 20634984, compound

https://huagongshe.com/reaction/49306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 20634926HCID 20634926—
SolventPyridineHCID 1049—
ProductHCID 20634984HCID 2063498468.9%

Reaction Steps

To a solution of 1,4-bis[5-(4-amino-3,5-dimethoxyphenyl)-2-pyridyl]hexahydro-1,4-diazepine tetrahydrochloride (40.0 mg, 0.0570 mmol), which was synthesized in Example 34, in pyridine (1.0 mL) was added methanesulfonyl chloride (30.0 mg, 0.260 mmol). The reaction mixture was stirred for 15 minutes, and concentrated under reduced pressure. A solution of the residue in methanol-chloroform (1:10) was washed with saturated aqueous sodium hydrogencarbonate and brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was recrystallized from chloroform-hexane to yield the title compound as a pale brown crystalline powder (melting point: 235.0-239.0° C.) (28.0 mg, yield: 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706703B2
Source datasetuspto-grants-2004_03
ORD IDord-447e9db61a4b489eaa870fbae088498b
Source noteuspto-grants-2004_03