HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 71115111, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 57389226 | HCID 57389226 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71115111 | HCID 71115111 | — |
Reaction Steps
Trifluoroacetic anhydride (50 mL) is added to a mixture of 4-[5-(4-carbamoyl-2-fluoro-phenyl)-2,3-dihydro-furo[2,3-c]pyridin-2-yl]-piperidine-1-carboxylic acid tert-butyl ester (50 mg) and triethylamine (100 mL) in dichloromethane (3 mL) and the reaction mixture is stirred at room temperature for 1 h. Aqueous NaHCO3 solution is added and the mixture is extracted with dichloromethane. The combined extracts are washed with brine, dried over MgSO4, and concentrated in vacuo. The residue is triturated with diethyl ether, stirred for 1 h, filtered off, and dried to give the title compound. LC (method 7): tR=1.47 min; Mass spectrum (ESI+): m/z=424 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08669271B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-a2cb76b943204da8acf87694b3a11cda |
| Source note | uspto-grants-2014_03 |