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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178481768 | HCID 178481768 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7,8-Dihydro-1-methyl-6H-pyrazolo[3',4':4,5]pyrimido[2,1-b]-[1,3]thiazin-4(1H)-one | HCID 22401671 | 38.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05527908 |
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| Source dataset | uspto-grants-1996_06 |
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| ORD ID | ord-c99c7185df5a4a24ad81fd0aff434707 |
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| Source note | uspto-grants-1996_06 |
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