HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 67959712, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 67959732 | HCID 67959732 | — |
| Product | HCID 67959712 | HCID 67959712 | 83% |
Reaction Steps
A mixture of (4R)-tert-butyl 4-(6-(5-bromo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-3-yl)pyrazin-2-yloxy)-6-azaspiro[2.5]octane-6-carboxylate (150 mg, 0.257 mmol), PdCl2dppf (20.96 mg, 0.026 mmol), and potassium acetate (76 mg, 0.770 mmol) in MeOH (2566 μL) was placed in a Symyx/Argonaut reactor for 16 h at 90° C. under CO (70 psi) when clean conversion was observed via 1 cms. The crude was purified via automated flash chromatography (silica gel) with 100% hexanes to 20% EtOAc/hexanes to give methyl 3-(6-((R)-6-(tert-butoxycarbonyl)-6-azaspiro[2.5]octan-4-yloxy)pyrazin-2-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-5-carboxylate (120 mg, 0.213 mmol, 83% yield) as a colorless oil. MS (ESI, pos. ion) m/z: 564.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09090593B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-050a6f115d7442349bb3c7898b31075d |
| Source note | uspto-grants-2015_07 |