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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300203Generated: November 1, 2026

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

https://huagongshe.com/reaction/2300203

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 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 elute 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 (M++H); HRMS Calcd. for C30H30N2O4S(M+): 514.1926. Found: 514.1927.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498170B2
Source datasetuspto-grants-2002_12
ORD IDord-3f96795c45904bdd99f58409049b951a
Source noteuspto-grants-2002_12