Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961544Generated: October 31, 2026

Triethylamine → HCID 56654398, compound

https://huagongshe.com/reaction/1961544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 86661739HCID 86661739—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 56654398HCID 5665439894%

Reaction Steps

To a solution of 5-(3-chloro-5-(trifluoromethyl)phenyl)-3-(4-(3-fluoroazetidin-3-yl)phenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazole (Preparation 22, 95 mg, 0.2 mmol) in CH2Cl2 (5 mL) was added triethylamine (0.15 mL, 1.1 mmol) and DMAP (5 mg, 0.04 mmol). Contents were stirred for 30 minutes at which time mesyl chloride (25 mg, 0.2 mmol) was added and the reaction was stirred for 18 hours at room temperature. Next, the reaction was concentrated to ˜3 mL under nitrogen purge and injected directly onto a 24 g Redi-Sep column. The crude material was chromatographed eluting from 100% heptane to 30:70 EtOAc:heptane to afford the final product (95 mg, 94%) as a solid. 1HNMR (CDCl3) δ ppm: 7.85 (1H), 7.79-7.77 (3H), 7.72 (1H), 7.64 (2H), 4.50-4.42, (2H), 4.34-4.27 (2H), 4.18 (1H), 3.76 (1H), 3.03 (3H); m/z (Cl) 545 ([M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415310B2
Source datasetuspto-grants-2013_04
ORD IDord-d719468a17a9427788f7e6ad751c903f
Source noteuspto-grants-2013_04