HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 57917659, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Amino-3-fluorobenzoic acid | HCID 9971 | — |
| Reactant | Propylphosphonic anhydride | HCID 111923 | — |
| Reactant | HCID 57917592 | HCID 57917592 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium bicarbonate ethyl acetate | HCID 86584982 | — |
| Product | HCID 57917659 | HCID 57917659 | 66.6% |
Reaction Steps
To a solution of N-cyclobutyl-3-(piperazin-1-ylmethyl)benzamide (8.78 mmol, 2.4 g), 4-amino-3-fluorobenzoic acid (8.78 mmol, 1.362 g) and triethylamine (26.3 mmol, 3.67 mL, 2.67 g) in dichloromethane (50 mL) was added 1-propanephosphonic acid cyclic anhydride (13.17 mmol, 7.84 mL, 8.38 g, 50% solution in ethyl acetate). The reaction was stirred for 1 hour then was diluted with ethyl acetate/sodium hydrogen carbonate (aqueous). The organic layer was separated, dried (magnesium sulfate) and concentrated under reduced pressure to give the title compound (2.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08314091B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-25fd4cfa5d2c4162ba2259bef6597ed2 |
| Source note | uspto-grants-2012_11 |