Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 89995666 | HCID 89995666 | — |
| Reactant | HCID 89996058 | HCID 89996058 | — |
| Solvent | tetrahydrofuran N-methylpyrrolidinone | HCID 22156051 | — |
| Product | HCID 73388519 | HCID 73388519 | 14% |
Reaction Steps
A suspension of NaH (4.3 mg), 2-methyl-1-(4-(2-(methylsulfonyl)pyrido[2,3-d]pyrimidin-7-yl)-1H-pyrazol-1-yl)propan-2-ol (Preparation 69, 15.5 mg, 0.045 mmol), N-(4-(1,2-dimethyl-1H-imidazol-5-yl)-2-methoxyphenyl)formamide (Preparation 74, 16.4 mg, 0.067 mmol) in NMP/THF (1/3 mL) was stirred at 160° C. under microwave irradiation for 2 hours. The reaction mixture was filtered, diluted with NaCl solution and extracted with EtOAc. The EtOAc portion was purified by elution through an SCX-2 column using 2M NH3/MeOH to give the title compound as yellow oil (3 mg, 14%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09334286B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-44057c07e57c47a7baee29f5621d2b30 |
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| Source note | uspto-grants-2016_05 |
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