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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527911Generated: November 1, 2026

4-Cyanobenzenesulfonyl chloride → HCID 56837010, compound

https://huagongshe.com/reaction/527911

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Cyanobenzenesulfonyl chlorideHCID 39497—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 68027120HCID 68027120—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 56837010HCID 5683701026%

Reaction Steps

To a solution of (R)—N-methyl-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrrolidin-3-amine (30 mg, 0.138 mmol) in THF (2 mL) were added 4-cyanobenzene-1-sulfonyl chloride (42 mg, 0.208 mmol) and DIPEA (36 mg, 0.28 mmol). The reaction mixture was stirred at room temperature for 0.5 hour. The reaction mixture was then diluted with water, and extracted with EtOAc. The organic layers were combined, dried, and concentrated. The residue was purified by preparative TLC to give the title compound (13.6 mg, 26%). MS (m/z): 383 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346810B2
Source datasetuspto-grants-2016_05
ORD IDord-0841da6736134012a62e162d6b3a4074
Source noteuspto-grants-2016_05