Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703842Generated: November 1, 2026

Methanol → HCID 14254434, compound

https://huagongshe.com/reaction/703842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantHCID 14254433HCID 14254433—
ProductHCID 14254434HCID 1425443470%

Reaction Steps

Three (3) grams of the thus obtained 2-benzylthio-7-chloro-6-nitro-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one was dissolved in 50 ml of methanol, and 0.8 g of pyridine was added. The solution was stirred under refluxing for 30 minutes. After the reaction was finished, the reaction mixture was cooled and poured into water. The resulting mixture was extracted with toluene. The organic layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the residue was washed with isopropyl ether. Thus, 2.1 g of 2-benzylthio-7-methoxy-6-nitro-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one was obtained. Yield 70%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04985432
Source datasetuspto-grants-1991_01
ORD IDord-9ed803171a2b4fce9a58a4a389428f70
Source noteuspto-grants-1991_01