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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966459Generated: October 30, 2026

Triethylamine → 2-(benzylamino)-N-methyl-4-(4-benzoylpiperazin-1-yl)benzamide

https://huagongshe.com/reaction/1966459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant2-(Benzylamino)-4-(4-benzoylpiperazin-1-yl)benzoic acidHCID 58425660—
ReactantMethylamine tetrahydrofuranHCID 66615946—
SolventTetrahydrofuranHCID 8028—
Product2-(benzylamino)-N-methyl-4-(4-benzoylpiperazin-1-yl)benzamideHCID 6718188636%

Reaction Steps

A solution of 2-(benzylamino)-4-(4-benzoylpiperazin-1-yl)benzoic acid (80 mg, 0.2 mmol), 2 M methylamine THF solution (0.96 ml, 1.9 mmol), triethylamine (0.08 ml, 0.57 mmol) and diphenylphosphoryl azide (0.045 ml, 0.2 mmol) in 15 ml THF was stirred for 16 hours. The run was quenched with 1 ml water and all the solvents were evaporated under vacuum. 2-(benzylamino)-N-methyl-4-(4-benzoylpiperazin-1-yl)benzamide (30 mg, 36%) was obtained by flash column chromatograph (60% ethyl acetate in hexanes). 1H NMR (500 MHz, CDCl3) δ (ppm) 2.97 (d, 3H), 3.14-3.25 (d, br, 4H), 3.65 (s, br, 2H), 3.72 (s, br, 2H), 4.42 (d, 2H), 6.01 (d, J=2.3 Hz, 2H), 6.15 (dd, J=2.3, 8.7 Hz, 1H), 7.26-7.49 (m, 10H), 8.52 (s, 1H). 13C NMR (125 MHz, CDCl3): δ (ppm) 26.9, 47.8, 48.9, 98.3, 103.4, 107.5, 127.5, 127.6, 129.0, 129.1 130.4, 136.0, 139.7, 151.6, 154.3, 170.6, 170.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420640B2
Source datasetuspto-grants-2013_04
ORD IDord-b6a417b14e064bf998c826e6e45fc795
Source noteuspto-grants-2013_04