Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyanuric fluoride | HCID 12664 | — |
| Reactant | HCID 178492656 | HCID 178492656 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 58500434 | HCID 58500434 | — |
Reaction Steps
To a solution of 6-{[2-(3-chloro-pyridin-2-yl)-5-methoxy-2H-pyrazole-3-carbonyl]-amino}-5-methyl-2H-indazole-7-carboxylic acid isopropyl amide (0.300 g, 0.641 mmol) in chloroform (2.0 ml) was added cyanuryl fluoride (2,4,6-trifluoro-1,3,5-triazine) (0.220 g, 1.669 mmol) followed by triethylamine (0.090 ml, 0.046 mmol). The reaction mixture was stirred at 20° C. for three hours, then evaporated to dryness and submitted to high vacuum. The residue was taken up in a small amount of chloroform and separated from some less soluble material, then evaporated to give the compound showing the physical data described in the table under P.43.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598078B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-2e9c62cca85d4d748b3ab56ac0a2c3fb |
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| Source note | uspto-grants-2013_12 |
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