HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 69665633, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 86590934 | HCID 86590934 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69665633 | HCID 69665633 | 25% |
Reaction Steps
A solution of 3-(3-isocyanatomethyl-3H-isobenzofuran-1-ylidene)-1,3-dihydro-indol-2-one (95 mg, 0.31 mmol) and piperidine (92.8 μl, 0.94 mmol) in THF (2.0 ml) was stirred at room temperature for 4 hours. The reaction was partitioned between EtOAc and water. The organic layer was washed with dilute HCl aqueous solution, water, saturated NaHCO3 aqueous solution, water, brine, dried with anhydrous Na2SO4, and rotary evaporated to a brown film. The brown film was chromatographed through silica gel column (CHCl3 to 4% MeOH/CHCl3 gradient) to produce piperidine-1-carboxylic acid [3-(2-oxo-1,2-dihydro-indol-3-ylidene)-1,3-dihydro-isobenzofuran-1-ylmethyl]-amide as a yellow solid (30 mg, 25%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07060844B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-05260c46fa9846e08648d722f171fba9 |
| Source note | uspto-grants-2006_06 |