HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → [1,1'-Biphenyl]-4-acetamide, N-[(3-fluorophenyl)methyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Felbinac | HCID 3332 | — |
| Reactant | 3-Fluorobenzylamine | HCID 66853 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [1,1'-Biphenyl]-4-acetamide, N-[(3-fluorophenyl)methyl]- | HCID 11702481 | 33.2% |
Reaction Steps
To a solution of 4-biphenyl acetic acid (2.00 g, 9.42 mmol) in DMF (20 ml) was added DIEA (3.29 ml, 18.84 mmol) and stirred at room temperature for 15 min, then PyBOP (4.90 g, 9.42 mmol) added and the stirring continued for further 30 min, then 3-fluorobenzylamine (1.18 g, 9.42 mmol) added and the stirring continued for 24 hrs, then the reaction mixture poured on to ice cooled water acidified with (10 ml) 1 N HCl and extracted with ethyl acetate (100 ml) and the organic layer washed with saturated solution of NaHCO3, water and brine, dried over Na2SO4 and the solvent removed under vacuum to give a white powder of the desired compound (1.00 g) 33% yield. Another method involves the acid chloride coupling method described below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08980890B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-5740052273004bf9828dfdca8784c701 |
| Source note | uspto-grants-2015_03 |