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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569744Generated: October 27, 2026

Pyridine → HCID 20146254, compound

https://huagongshe.com/reaction/569744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonamide, N-sulfinyl-HCID 10931522—
ReactantMethyl 3-sulphinylamino-4-methylbenzoateHCID 20146257—
SolventBenzeneHCID 241—
ProductHCID 20146254HCID 20146254—

Reaction Conditions

Temperature0 °C

Reaction Steps

51.6 g (0.365 mole) of N-sulphinylmethanesulphonamide in 50 ml of benzene are added to a solution of 60 g (0.298 mole) of methyl 3-sulphinylamino-4-methylbenzoate in 200 ml of benzene at room temperature under argon. Thereafter, 24.9 g (0.315 mole) of pyridine, dissolved in 75 ml of benzene, are added in portions to the reaction mixture, while cooling with ice. The mixture is subsequently stirred at 0° C. for 10 minutes and then heated under reflux for 45 hours. After cooling, the benzene and pyridine are distilled off in vacuo, the oil which remains is poured into 150 ml of water and the mixture is acidified to pH 4 with 2N HCl. A brown solid thereby forms from the oil, and is extracted with chloroform. The chloroform extracts are washed with water, dried over MgSO4 and concentrated to dryness. The oil which remains crystallizes to a brown-yellow material by adding n-hexane, and the material is filtered off with suction and washed with n-hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04734407
Source datasetuspto-grants-1988_03
ORD IDord-b10e22ba1b024a4f94e667768c2f2260
Source noteuspto-grants-1988_03