Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyclobutylamine | HCID 75645 | — |
| Reactant | HCID 86646911 | HCID 86646911 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68514809 | HCID 68514809 | — |
Reaction Steps
A mixture of 3-(2-chloro-4-pyrimidinyl)-2-(4-fluorophenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridine (i.e. the product of Step B) (200 mg, 0.54 mmol), triethylamine (55 mg, 0.54 mmol) and cyclobutylamine (5.0 mL) was stirred at 65° C. for 18 h. The reaction mixture was diluted with dichloromethane (50 mL) and treated with silica gel (20.0 g). The silica gel suspension was concentrated under reduced pressure to leave a mixture of silica gel and crude product, which was purified by silica gel chromatography using a gradient of ethyl acetate/hexanes (1:9 to 1:0) as eluant to give 70 mg of the title product, a compound of the present invention, as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08288375B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-95c18468cd984c91a3b95eea290e72b0 |
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| Source note | uspto-grants-2012_10 |
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