Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | HCID 67314553 | HCID 67314553 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67314690 | HCID 67314690 | 85% |
Reaction Steps
A solution of 5-fluoro-3-(2-vinyl-7H-furo[3,4-b]pyridin-5-ylidene)-1,3-dihydro-indol-2-one (50 mg, 0.17 mmol) in dioxane (10 mL) is treated with 4-hydroxypiperidine (260 mg, 2.57 mmol) and 10 drops of glacial AcOH. The reaction is stirred at 100° C. for 1 h and then cooled to room temperature. The reaction mixture is treated with triethylamine (2 mL) and is loaded onto silica gel. Purification by chromatography (silica gel) gave the title compound (57 mg, 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07977351B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-d3eea84efedb45c8835f5dd8521692e4 |
|---|
| Source note | uspto-grants-2011_07 |
|---|