Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Pentanamine | HCID 12019 | — |
| Reactant | HCID 25212520 | HCID 25212520 | — |
| Product | HCID 59437546 | HCID 59437546 | 41.9% |
Reaction Steps
The title compound was prepared following procedure and work up described for example 118, but starting from N-[5-chloro-7-(trifluoromethyl)[1,2,4]triazolo[1,5-a]pyridin-2-yl]nicotinamide ((B7), 50 mg; 0.14 mmol; 1.0 eq) and 3-aminopentane (86 μL; 0.73 mmol; 5.0 eq), heated at 120° C., to give the title compound as a white solid (23 mg, 40%). HPLC, Rt: 3.66 min. (purity 96%). LC/MS, M+(ESI): 392.9, M−(ESI): 391.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08263595B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-f7123cf789234cfcbe065c8cb78ab3ac |
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| Source note | uspto-grants-2012_09 |
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