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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416049Generated: October 29, 2026

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

https://huagongshe.com/reaction/2416049

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 (Washburn, W. N., et al., EP 0 659 737) (17.0 g, 42.8 mmol) was dissolved in 200 mL of dimethylformamide 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(M30 ): 514.1926. Found: 514.1927.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06821991B2
Source datasetuspto-grants-2004_11
ORD IDord-b46a90c2fdc74b569880fef782adf006
Source noteuspto-grants-2004_11