HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 57917587, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Propylphosphonic anhydride | HCID 111923 | — |
| Reactant | 4-Amino-2,5-difluorobenzoic acid | HCID 20151477 | — |
| Reactant | N-tert-butyl-3-(piperazin-1-ylmethyl)benzamide | HCID 66877987 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57917587 | HCID 57917587 | 76.8% |
Reaction Steps
1-Propanephosphonic acid cyclic anhydride (2.91 g, 9.2 mmol, 2.73 mL) was added dropwise to a solution of 4-amino-2,5-difluorobenzoic acid (792.9 mg, 4.6 mmol), N-tert-butyl-3-(piperazin-1-ylmethyl)benzamide (1.3878 g, 5 mmol) and triethylamine (1.39 g, 13.9 mmol, 1.91 mL) in dichloromethane. The reaction mixture was stirred at room temperature for 1 hour. The reaction was concentrated under reduced pressure and the residue was taken up with ethyl acetate, washed with water, sodium hydrogen carbonate and brine. The organic phase was concentrated under vacuum to afford the title compound (1.52 g). MS (ESI) m/z 431.9 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08314091B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-e3b6d56a9b634a87ab0e28badff3be04 |
| Source note | uspto-grants-2012_11 |