Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | HCID 86608612 | HCID 86608612 | — |
| Catalyst | Tetraethylammonium cyanide | HCID 3014735 | — |
| Product | HCID 68636966 | HCID 68636966 | — |
Reaction Steps
A mixture of 5-chloro-6-(2-chloro-4-fluorophenyl)-7-(4-methylpiperidin-1-yl)-[1,2,4]-triazolo-[1,5-a]-pyrimidine (0.1 mol) and tetraethylammonium cyanide (0.25 mol) in 750 ml Dimethylformamide (DMF) was stirred for 16 hours at 20 to 25° C. To this mixture was added water and methyl-tert. butylether (MTBE), the organic phase was separated, washed with water, dried and filtered. The filtrate was evaporated and the residue was purified by column chromatography to yield 5.91 g of the title compound of mp. 247° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07763622B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-f241727ddaab4f4a84a22fdf6ddd9d0e |
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| Source note | uspto-grants-2010_07 |
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