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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32094Generated: October 26, 2026

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

https://huagongshe.com/reaction/32094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(7-cyanomethyl-chroman-4-yl)-3-phenyl-3-(3-trifluoromethyl-benzenesulfonylamino)-propionamideHCID 68932619—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Productn-[7-(2-Aminoethyl)-chroman-4-yl]-3-phenyl-3-(3-trifluoromethylbenzenesulfonylamino)-propionamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425631B2
Source datasetuspto-grants-2008_09
ORD IDord-d04f5765686e4e7f9150a96136bcd820
Source noteuspto-grants-2008_09