Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromopropane | HCID 6358 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178515422 | HCID 178515422 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 56630726 | HCID 56630726 | 55.8% |
Reaction Steps
A mixture of 0.9 g (0.0042 moles) of 3-(1H-tetrazol-5-yl)-4-oxo-4H-pyrido[1,2-a]pyrimidine, 25 ml of dimethylformamide, 1.15 g (0.0084 moles) of anhydrous potassium carbonate and 1.1 ml (0.0126 moles) of isopropyl bromide was stirred at 90° C. for 1 hour. The hot yellow solution was filtered, the filtrate evaporated. To the crystalline residue 25 ml of water was added, and the crystals were collected. 0.6 g (55.8%) of the title compound was obtained, in the form of white crystals, m.p.: 146°-148° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05475000 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-e5f4d57f8fac49309363d2511fa8c3ba |
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| Source note | uspto-grants-1995_12 |
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