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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374570Generated: October 31, 2026

Pyridine → HCID 19438397, compound

https://huagongshe.com/reaction/374570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSodium CyanateHCID 517096—
Reactant1-methyl-4-ethoxycarbonylpyrazole-5-sulfonylchlorideHCID 10977963—
SolventAcetonitrileHCID 6342—
ProductHCID 19438397HCID 19438397—

Reaction Conditions

Temperature40 °C

Reaction Steps

1.08 g (16.6 mmole) of anhydrous sodium cyanate, 1.25 g (15.8 mmole) of dry pyridine and 20.0 g of dry acetonitrile were mixed together and the resulting mixture was then stirred under nitrogen atmosphere while maintaining the temperature of 40° C. To this mixture was added 3.80 g (15.0 mmole) of 4-ethoxycarbonyl-1-methylpyrazole-5-sulfonylchloride over one hour. The reaction mixture was then stirred for further 2 hours while maintaining the temperature of 40° to 45° C. to complete the reaction. After the reaction was completed, the reaction solution was filtered under nitrogen atmosphere. The solvent and the remaining pyridine were removed from the filtrate at normal temperature by means of a vacuum pump to obtain the crude product which was then washed with 10.00 g of dry ethyl ether and dried to obtain 4.68 g (Yieid 92%) of the title compound as the white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05480993
Source datasetuspto-grants-1996_01
ORD IDord-cde20ef7a57f4228aeb7ead0eb08fc11
Source noteuspto-grants-1996_01