Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260522Generated: October 26, 2026

1,3-Dibromopropane → 7,8-Dihydro-1-methyl-6H-pyrazolo[3',4':4,5]pyrimido[2,1-b]-[1,3]thiazin-4(1H)-one

https://huagongshe.com/reaction/260522

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromopropaneHCID 8001—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178481768HCID 178481768—
SolventDimethylformamideHCID 6228—
Product7,8-Dihydro-1-methyl-6H-pyrazolo[3',4':4,5]pyrimido[2,1-b]-[1,3]thiazin-4(1H)-oneHCID 2240167138.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

In 80 ml of dimethylformamide was dissolved 4.0 g (22.0 mmol) of 4,5-dihydro-6-mercapto-1-methylpyrazolo[3,4-d]pyrimidin-4(1H)-one [Helv. Chim. Acta, 42, 349 (1959)], and 9.1 g (66 mmol) of potassium carbonate and 3.34 ml (32.9 mmol) of 1,3-dibromopropane were added to the solution, followed by stirring at 80° C. for 8 hours. After evaporation of the solvent, the residue was subjected to partition between chloroform and water, and the chloroform layer was concentrated to dryness under reduced pressure. The residue was subjected to silica gel column chromatography and eluted with chloroform-methanol (100:1) to give 1.87 g (38%) of Compound 44. The compound was recrystallized from ethanol for purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05527908
Source datasetuspto-grants-1996_06
ORD IDord-c99c7185df5a4a24ad81fd0aff434707
Source noteuspto-grants-1996_06