Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4,4,4-Trifluorobutylamine | HCID 136645 | — |
| Reactant | HCID 11001647 | HCID 11001647 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131725933 | HCID 131725933 | 73.5% |
Reaction Steps
A solution of 1.5 mmol 1,1,1-trifluorobutane-4-amine, 1.5 mmol triethylamine in 10 ml dichloromethane is added to a solution of 1.5 mmol 5,7-dichloro-6-(2-chloro-6-fluorophenyl)-[l,2,4]-triazolo[1,5-α]pyrimidine [cf. EP-A 550 113] in 20 ml dichloromethane. The combined solution was stirred for about 16 hours at 20 to 25° C. and subsequently washed with diluted (5%) hydrochloric acid. The organic phase was separated, dried and filtered. Distillative removal of the solvent from the filtrate and chromatography over silica gel yielded 0.45 g of the title compound of mp. 115° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07105664B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-c22c748f82a8427bba1f54d8a6ce4bd1 |
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| Source note | uspto-grants-2006_09 |
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