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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423173Generated: October 30, 2026

Pyridine → HCID 178494712, compound

https://huagongshe.com/reaction/423173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethoxyacetic AcidHCID 12251—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantN-MethylhydrazinecarbothioamideHCID 2723853—
SolventDimethylformamideHCID 6228—
ProductHCID 178494712HCID 178494712192.4%

Reaction Steps

5 g of methoxy-acetic acid (55.5 mmol) were dissolved in 70 ml of dimethylformamide. 11.73 g of 1,1′-carbonyldiimidazol (72.3 mmol) were added in portions within 10 min. After 30 min. at room temperature 23 ml of pyridine were added. Then 5.84 g of 4-methyl-3-thiosemicarbazide (55.5 mmol) were added and the obtained solution was stirred at room temperature overnight, and for an additional 3 h at 100° C. The solvent was evaporated, the residue dissolved in 70 ml of saturated aqueous sodium chloride solution and 30 ml of water. The aqueous layer was extracted six times with 100 ml of ethyl acetate each, and the combined organic layers were dried over magnesium sulfate, filtered, and the solvent was evaporated to dryness to yield 17 g of the crude title compound, which was further purified by silica gel chromatography with ethyl acetate, thereby obtaining 7.1 g of the purified title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101754B2
Source datasetuspto-grants-2012_01
ORD IDord-d389c364866544718146e19c4853c785
Source noteuspto-grants-2012_01