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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977984Generated: October 25, 2026

3,4-Dimethoxy-1,2,5-thiadiazole 1-oxide → 3-Methoxy-4-[7-(piperidino)hept-5-ynylamino]-1,2,5-thiadiazole-1-oxide

https://huagongshe.com/reaction/977984

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dimethoxy-1,2,5-thiadiazole 1-oxideHCID 12913947—
Reactant7-Piperidinohept-5-ynylamineHCID 20147643—
SolventMethanolHCID 887—
Product3-Methoxy-4-[7-(piperidino)hept-5-ynylamino]-1,2,5-thiadiazole-1-oxideHCID 20147656—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 3,4-dimethoxy-1,2,5-thiadiazole-1-oxide (2.0 g) in methanol (100 ml) was cooled to 0° C. 7-(Piperidino)hept-5-ynylamine (2.5 g) in methanol (50 ml) was added dropwise with stirring over 30 minutes maintaining the reaction temprature at 0° C. The reaction mixture was stirred at 0° C. for a further 2 hours to give a solution of 3-methoxy-4-[7-(piperidino)hept-5-ynylamino]-1,2,5-thiadiazole-1-oxide. Ammonia gas was bubbled through this solution for 30 minutes and the mixture allowed to stand for 16 hours. The reaction mixture was evaporated under reduced pressure to give an oil which was taken up in ethyl acetate, triturated and cooled to give the title compound (3.0 g), m.p. 134°-6° C. (recrystallisation from isopropanol-ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04663331
Source datasetuspto-grants-1987_05
ORD IDord-572cb061cf4f41a0b681814322d23934
Source noteuspto-grants-1987_05