Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 18418759 | HCID 18418759 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23388399 | HCID 23388399 | 93.3% |
Reaction Steps
To a solution of 1,1′-carbonyldiimidazole (3.4 g, 21 mmol) in 60 mL of dry THF was added dropwise a solution of 1-phenyl-1H-indazole-3-carboxylic acid (5.0 g, 21 mmol) in 60 mL dry THF under nitrogen atmosphere. The resulting reaction mixture was stirred at ambient temperature for 30 minutes and refluxed for 30 minutes; then cooled to ambient temperature under nitrogen atmosphere. Ammonia, generated by warming concentrated aqueous ammonia solution, was bubbled through, and the reaction mixture was stirred overnight at ambient temperature. The reaction mixture was concentrated in vacuo to dryness, the solid was dissolved in 200 mL of ethyl acetate, the solution was successively washed with 1N aqueous HCl solution (2×50 mL), 1N aqueous NaOH solution (5×20 mL) and was dried over Na2SO4. Concentration and drying under vacuum gave 4.65 g (93%) of desired product as a white solid: mp 149° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06458781B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-04a10af7cb374fbe971c195a3a836099 |
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| Source note | uspto-grants-2002_10 |
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