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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794704Generated: November 2, 2026

Dibenzylamine → N-[2-Benzyloxy-5-(2-dibenzylamino-1-oxo-ethyl)-phenyl]-methanesulfonamide

https://huagongshe.com/reaction/1794704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibenzylamineHCID 7656—
ReactantN-[2-Benzyloxy-5-(2-chloro-1-oxo-ethyl)-phenyl]-methanesulfonamideHCID 22220311—
SolventDimethylformamideHCID 6228—
ProductN-[2-Benzyloxy-5-(2-dibenzylamino-1-oxo-ethyl)-phenyl]-methanesulfonamideHCID 22220380—

Reaction Steps

N-[2-Benzyloxy-5-(2-chloro-1-oxo-ethyl)-phenyl]-methanesulfonamide (EP 0 659 737) (17.0 g, 42.8 mmol) was dissolved in 200 mL of N,N-dimethylformamide (DMF) and treated with dibenzylamine (22.0 g, 110 mmol). The mixture was stirred at room temperature overnight and then the solvent was removed. The residue was purified by silica gel chromatography using 20–50% ethyl acetate/hexanes as eluent to give the title compound as a white solid; 1H NMR (300 MHz, CDCl3) δ 2.94 (s, 3 H), 3.77 (s, 2 H), 3.82 (s, 2 H), 5.16 (s, 2 H), 6.75 (brs, 1 H), 6.96 (d, J=8.7 Hz, 1 H), 7.20–7.50 (m, 15 H), 7.67 (dd, J=8.7, 2.1 Hz, 1 H), 8.10 (d, J=2.1 Hz, 1 H); MS (ES) m/z: 515.2 (MH+); HRMS Calcd. for C30H30N2O4S(M+): 514.1926. Found: 514.1927.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022716B2
Source datasetuspto-grants-2006_04
ORD IDord-40e13555e7644c7f81339486a2511127
Source noteuspto-grants-2006_04