Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 67517333 | HCID 67517333 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 67517760 | HCID 67517760 | 28.6% |
Reaction Steps
To N′-(8-(2-fluorobenzyl)-8-azabicyclo[3.2.1]octane-2-carbonyl)-3-(2-methylpyridin-4-yl)-1-trityl-1H-indazole-5-carbohydrazide (142 mg, 0.19 mmol) in acetonitrile (1.6 mL) was added pyridine (44 mg, 0.56 mmol), followed by phosphoryl trichloride (86 mg, 0.56 mmol). The reaction mixture was heated at 100° C. under microwave condition for 30 min. After quench with saturated NaHCO3, the mixture was extracted with EtOAc. The combined organic layer was dried and concentrated to give 40 mg crude product. The crude was brought to next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08999966B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-f1c57f2b6f654d9a83697b98f0acd9ee |
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| Source note | uspto-grants-2015_04 |
|---|