HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(7-cyanomethyl-chroman-4-yl)-3-phenyl-3-(3-trifluoromethyl-benzenesulfonylamino)-propionamide → n-[7-(2-Aminoethyl)-chroman-4-yl]-3-phenyl-3-(3-trifluoromethylbenzenesulfonylamino)-propionamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(7-cyanomethyl-chroman-4-yl)-3-phenyl-3-(3-trifluoromethyl-benzenesulfonylamino)-propionamide | HCID 68932619 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | n-[7-(2-Aminoethyl)-chroman-4-yl]-3-phenyl-3-(3-trifluoromethylbenzenesulfonylamino)-propionamide | HCID 68929539 | — |
Reaction Steps
To a solution of N-(7-cyanomethyl-chroman-4-yl)-3-phenyl-3-(3-trifluoromethyl-benzenesulfonylamino)-propionamide (790 mg, 1.45 mmol) in MeOH (20 mL) in the Parr-bottle was added Pd/C (80 mg) while flushed under N2. The reaction mixture bottle was placed in Parr-shaker. The H2 was filled up the bottle then released-this was done 3 times. After last release, the fresh H2 (50 psi) was then filled up the bottle. The reaction was under hydrogenation for 18 h. Solvent was separated from the Pd/C by passing through the Celite®. Solvent was evaporated in vacuo to give the final product. MS m/z: 548.12 (M+H). Calc'd. for C27H28F3N3O4S-547.06.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07425631B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-d04f5765686e4e7f9150a96136bcd820 |
| Source note | uspto-grants-2008_09 |