Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 68917727 | HCID 68917727 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | HCID 68921803 | HCID 68921803 | 81.1% |
Reaction Steps
To a solution of the compound obtained in Example 36 (24 mg) in methanol/tetrahydrofuran (2 mL/1 mL) was added sodium methoxide (23 mg) and the mixture was stirred at 100° C. for 2 hours in a microwave reactor. After cooling to room temperature, to the reaction mixture was added chloroform and water and the organic layer was separated and concentrated in vacuo and the resultant crude product was purified by a column chromatography on NH-silica gel (Chromatorex NH-silica gel/Fuji Silicia Chem., solvent; hexane/ethyl acetate=65/35 to 30/70) to give 6-(2-chlorophenyl)-7-(4-chlorophenyl)-3-(N-cyclopentylcarbamoyl)-2,5-dimethoxypyrazolo[1,5-a]pyrimidine (17.8 mg; yield: 81%) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188097B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-c1bbc7095f104b8e8e8a8bbf3bea2fe6 |
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| Source note | uspto-grants-2012_05 |
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