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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408122Generated: November 1, 2026

Cyclopropanesulfonamide → HCID 59053761, compound

https://huagongshe.com/reaction/2408122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanesulfonamideHCID 15765418—
ReactantHCID 70496256HCID 70496256—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 59053761HCID 5905376120.1%

Reaction Steps

A mixture of 2-[5-(4-tert-butyl-phenyl)-pyridin-3-yl]-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid (200 mg, 0.48 mmol), 1-3-dimethylaminopropyl-3-ethylcarbodiimide hydrochloride (130 mg, 0.72 mmol), 4-dimethylaminopyridine (88 mg, 0.72 mmol), cyclopropane sulfonic acid amide (170 mg, 1.44 mmol) in dichloromethane (20 mL) was refluxed for 12 h. Removal of the solvent to afford the oil residue. Purification by Waters automated flash system (column: Xterra 30 mm×100 mm, sample manager 2767, pump 2525, detector: ZQ mass and UV 2487, solvent system: acetonitrile and 0.1% formic acid in water) afforded cyclopropanesulfonic acid {2-[5-(4-tert-butyl-phenyl)-pyridin-3-yl]-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carbonyl}-amide (50 mg, 20%) as a light yellow solid: MS (ESI) M+1=518.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809369B2
Source datasetuspto-grants-2014_08
ORD IDord-7f8b0fb2deeb4c8fa2816f19add1dd12
Source noteuspto-grants-2014_08