HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 86761341, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | tert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylate | HCID 22135564 | — |
| Reactant | HCID 59822470 | HCID 59822470 | — |
| Product | HCID 86761341 | HCID 86761341 | 45% |
Reaction Steps
A solution of 1-isopropyl-5-methyl-2-oxo-N-(piperidin-4-ylmethyl)-1,2-dihydroquinoline-3-carboxamide (150 mg, 0.44 mmol, step 4 in preparation 3) and tert-butyl 1-oxa-6-azaspiro[2.5]octane-6-carboxylate (112 mg, 0.53 mmol, Castro Jose L. et al., J. Med. Chem., 1998, 41, 2667) in methanol (5 mL) was heated at 80° C. overnight. After cooled to room temperature, concentrated gave yellow oil. The residue was chromatographed on a column of silica gel eluting with 25% ammonium hydroxide/methanol/dichloromethane (2/10/100) to give 111 mg (45%) of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07964727B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-fb44c75cc00d4a618ebd8a9d70bbf593 |
| Source note | uspto-grants-2011_06 |