Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | HCID 25212520 | HCID 25212520 | — |
| Product | HCID 59437508 | HCID 59437508 | 29.3% |
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 ethanolamine (44 μL; 0.73 mmol; 5.0 eq), heated at 120° C., to give the title compound as a white solid (15 mg, 28%). HPLC, Rt: 1.91 min. (purity 97.9%). LC/MS, M+(ESI): 366.8, M−(ESI): 364.9.
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-844c7b7092914fdda26dcbd52fccf76e |
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| Source note | uspto-grants-2012_09 |
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