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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734960Generated: October 26, 2026

4-Cyanobenzenesulfonyl chloride → HCID 68505680, compound

https://huagongshe.com/reaction/734960

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Cyanobenzenesulfonyl chlorideHCID 39497—
Reactant5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinamineHCID 57843474—
SolventPyridineHCID 1049—
ProductHCID 68505680HCID 6850568067.2%

Reaction Steps

To a solution of 5-[3-(1-methyl-1H-pyrazol-4-yl)-6-quinoxalinyl]-3-pyridinamine (52 g, 0.172 mmol) in pyridine (1.7 mL) was added 4-cyanobenzenesulfonyl chloride (56 mg, 0.278 mmol). The reaction mixture was stirred at room temperature overnight. Monitoring by LCMS still showed 30% of starting material. An additional portion of 4-cyanobenzenesulfonyl chloride (17 mg, 0.084 mmol) was added to the reaction mixture and after stirring for a further 30 minutes, all starting material was consumed. Cold water was poured into the reaction resulting in precipitate formation. This solid was collected by filtration, washed with water and dried under vacuum to give the title compound (54 mg, 67%) as a brown colored solid. MS(ES)+ m/e 468 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592342B2
Source datasetuspto-grants-2009_09
ORD IDord-24956f82540e4fbf91abf0de6a01d6d0
Source noteuspto-grants-2009_09