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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898069Generated: October 30, 2026

Diisopropylethylamine → 4-Chloro-n[5-chloro-2-(cis-2,6-dimethyl-morpholine-4-carbonyl)-pyridin-3-yl]-n-methoxymethyl-3-trifluoromethyl-benzenesulfonamide

https://huagongshe.com/reaction/1898069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2,6-Dimethylmorpholine, cis-HCID 641500—
Reactant5-Chloro-3-[(4-chloro-3-trifluoromethyl-benzenesulfonyl)-methoxymethyl-amino]-pyridine-2-carbonyl chlorideHCID 57942241—
SolventDichloromethaneHCID 6344—
Product4-Chloro-n[5-chloro-2-(cis-2,6-dimethyl-morpholine-4-carbonyl)-pyridin-3-yl]-n-methoxymethyl-3-trifluoromethyl-benzenesulfonamideHCID 66649011—

Reaction Steps

A mixture of 5-chloro-3-[(4-chloro-3-trifluoromethyl-benzenesulfonyl)-methoxymethyl-amino]-pyridine-2-carbonyl chloride (50 mg, 0.11 mmol), cis-2,6-dimethylmorpholine (50 mg, 0.40 mmol) and di-isopropylethylamine (DIEA, 0.07 mL, 0.40 mmol) in CH2Cl2 (1.5 mL) was stirred at room temperature overnight. The mixture was concentrated to provide 4-chloro-N-[5-chloro-2-(cis-2,6-dimethyl-morpholine-4-carbonyl)-pyridin-3-yl]-N-methoxymethyl-3-trifluoromethyl-benzenesulfonamide, which was directly used in the next step without any purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519135B2
Source datasetuspto-grants-2013_08
ORD IDord-5eecf35d43b94cc7ab9500bc7b3116a6
Source noteuspto-grants-2013_08