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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968818Generated: October 27, 2026

Carbon Dioxide → (4-Amino-3-{[3-(cyclohexyl-methyl-amino)-propylamino]-methyl}-phenyl)-phenyl-methanone

https://huagongshe.com/reaction/1968818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantTetrahydrofuranHCID 8028—
ReactantThiopheneHCID 8030—
ReactantN-Methyl-1,3-propanediamineHCID 80511—
Reactant5-Benzoyl-2-nitrobenzaldehydeHCID 19816055—
CatalystPalladiumHCID 23938—
Product(4-Amino-3-{[3-(cyclohexyl-methyl-amino)-propylamino]-methyl}-phenyl)-phenyl-methanoneHCID 58625047—

Reaction Steps

A mixture of 5-benzoyl-2-nitrobenzaldehyde. (0.0058 mol) in THF (100 ml) was hydrogenated with 10% Pd/C (1 g) as a catalyst in the presence of 4% thiophene solution (1 mL). After uptake of H2 (3 equiv), the mixture was put in an autoclave. N-cyclohexyl, N-methyl-propane-1,3-diamine (0.01 mol) and CaH2 (0.5 g) were added and the mixture was reacted under 10 atm of CO2 and 50 atm of H2 at 50° C. for 16 hours. When the reaction was complete, the mixture was purified over silica gel on a glass filter (eluent: 90:10 CH2Cl2:(CH3OH:NH3)). The product fractions were collected and the solvent was evaporated to yield the title compound as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426429B2
Source datasetuspto-grants-2013_04
ORD IDord-46f5c54e49a84ce6bd2d1e5b3e7634bf
Source noteuspto-grants-2013_04