Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 5-Amino-3-isopropyl-1-(2,4,6-trichlorophenyl)pyrazole-4-carboxamide | HCID 18540630 | — |
| Reactant | Ethyl 3-aminoindazol-5-ylacetate | HCID 18540672 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178440265 | HCID 178440265 | — |
Reaction Steps
To a stirred solution of 139 mg (0.40 mmol) of 5-amino-3-isopropyl-1-(2,4,6-trichlorophenyl)pyrazole-4-carboxamide in 3 mL of absolute ethanol was added 329 mg (1.50 mmol) of ethyl 3-aminoindazol-5-ylacetate followed by 1.13 mL (3.0 mmol) of 2.66 M sodium ethoxide in ethanol. The solution was stirred 16 h at reflux, and the heating mantle was then removed. The reaction was treated with 8 mL of 10% aq. HOAc, poured into water, and extracted with EtOAc. The organic extract was washed with brine, dried (MgSO4), concentrated under reduced pressure, and chromatographed on silica gel (gradient elution with 5% to 10% MeOH—CH2Cl2) to give, after removal of solvent, 123 mg (61%) of 1-(2,4,6-trichlorophenyl)-3-isopropyl-6-(3-aminoindazol-5-ylmethyl)pyrazolo[3,4-d]pyrimidin-4-one as a white, amorphous solid. Mass spec.: 502.0712 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06531477B1 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-b0e726281b794c7d91327139985e7fc5 |
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| Source note | uspto-grants-2003_03 |
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