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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366064Generated: October 31, 2026

Triethylamine → HCID 28376252, compound

https://huagongshe.com/reaction/2366064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Pyridinamine, N-methyl-HCID 20727—
Reactant2-Chloro-5-pyridinesulfonyl chlorideHCID 2792792—
SolventDichloromethaneHCID 6344—
ProductHCID 28376252HCID 28376252—

Reaction Steps

To a solution of 1.3 g (11.8 mmol) of N-methylpyridin-2-amine in 25 mL of DCM are added, at 0° C., 3.3 mL (23.6 mmol) of triethylamine and then, portionwise, 2.5 g (11.8 mmol) of 6-chloropyridine-3-sulfonyl chloride (prepared according to document WO 98/40332). After stirring for 12 hours at room temperature, the reaction medium is taken up in 100 mL of DCM, washed successively with 100 mL of water and 30 mL of brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue obtained is purified by chromatography on a column of silica gel, eluting with a 4/1 cyclohexane/EtOAc mixture. After concentrating under reduced pressure, 2.8 g of 6-chloro-N-methyl-N-pyridin-2-ylpyridine-3-sulfonamide are obtained in the form of a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697731B2
Source datasetuspto-grants-2014_04
ORD IDord-6f3f7d7840674db9ac0c229cd80a9ca7
Source noteuspto-grants-2014_04