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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199103Generated: November 1, 2026

Tripropylamine → 7-chloro-2-(2-cyclohexylethyl)-6-nitro-5H-[1,3,4]thiadiazolo[3,2-a]pyrimidin-5-one

https://huagongshe.com/reaction/1199103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTripropylamineHCID 7616—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-(2-cyclohexylethyl)-7-hydroxy-6-nitro-5H-[1,3,4]thiadiazolo[3,2-a]pyrimidin-5-oneHCID 135457327—
Product7-chloro-2-(2-cyclohexylethyl)-6-nitro-5H-[1,3,4]thiadiazolo[3,2-a]pyrimidin-5-oneHCID 10315376—

Reaction Steps

In 30 ml of phosphorous oxychloride was suspended 10.2 g of 2-(2-cyclohexylethyl)-7-hydroxy-6-nitro-5H-[1,3,4]thiadiazolo[3,2-a]pyrimidin-5-one, and 4 ml of tripropylamine was added dropwise to the suspension at room temperature while stirring. The stirring was continued at 80° to 85° C. for an additional 3 hours. After cooling, the reaction mixture was poured into ice-water, and the precipitate formed was collected by filtration and washed with water to obtain 10.4 g of 7-chloro-2-(2-cyclohexylethyl)-6-nitro-5H-[1,3,4]thiadiazolo[3,2-a]pyrimidin-5-one as a crystalline powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04898943
Source datasetuspto-grants-1990_02
ORD IDord-a6ca99b04a6b494c8c5dbd0e333770c8
Source noteuspto-grants-1990_02