Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979246Generated: October 30, 2026

Pyridine → N-[[[4-[2-chloro-4-(trifluoromethyl)phenoxy]-2-fluorophenyl]amino]thio]-N-methylbutanamide

https://huagongshe.com/reaction/979246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSulfur dichlorideHCID 25353—
ReactantN-MethylbutanamideHCID 28774—
ReactantBenzenamine, 4-[2-chloro-4-(trifluoromethyl)phenoxy]-2-fluoro-HCID 15595105—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductN-[[[4-[2-chloro-4-(trifluoromethyl)phenoxy]-2-fluorophenyl]amino]thio]-N-methylbutanamideHCID 2018387783.8%

Reaction Conditions

Temperature10 °C

Reaction Steps

A solution of sulphur dichloride (11.3 g) in dichloromethane (10 ml) was added over 20 minutes to a solution of N-methylbutanamide (10.1 g) in the same solvent (35 ml) with stirring, the temperature being maintained at 10° C. Stirring at this temperature was continued for a further 30 minutes after which time a solution of pyridine (8.7 g) in dichloromethane (15 ml) was added. The mixture was then stirred and allowed to warm to room temperature over 2 hours, then filtered. The solvent was stripped off and the residue extracted with diethyl ether. After filtration, solvent removal and distillation, 12.1 g of the sulphenyl chloride as an oil, boiling point 82°-84° C. at 13 mmHg, was obtained. 4.4 g of this oil was dissolved in diethyl ether (10 ml) and the resulting solution was added over 20 minutes to a mixture of the compound of Example 1 (7.6 g) and triethylamine (2.7 g) in diethyl ether (30 ml). After stirring for 30 minutes at room temperature, 150 ml diethyl ether was added, the resultant soution was washed three times with water, dried, stripped of solvent and purified by chromatography over silica using dichloromethane as eluant. 9.1 g of the desired product was obtained as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04666942
Source datasetuspto-grants-1987_05
ORD IDord-3ddb8084f71e4fdb8f92805fa8f5869e
Source noteuspto-grants-1987_05