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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966461Generated: October 30, 2026

P,P-Diphenylphosphinic azide → HCID 46200788, compound

https://huagongshe.com/reaction/1966461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantEthanol, reaction products with ammonia, distn. residuesHCID 22020343—
Reactant2-(Benzylamino)-4-(4-benzoylpiperazin-1-yl)benzoic acidHCID 58425660—
SolventTetrahydrofuranHCID 8028—
ProductHCID 46200788HCID 4620078848.3%

Reaction Steps

A solution of 2-(benzylamino)-4-(4-benzoylpiperazin-1-yl)benzoic acid (80 mg, 0.2 mmol), 2 M ammonia ethanol solution (0.60 ml, 1.2 mmol), tiethylamine (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)-4-(4-bezoylpiperazin-1-yl)benzamide (40 mg, 40%) was obtained by flash column chromatograph (60% ethyl acetate in hexanes), and its hydrochloride was made by bubbling HCL gas in ether solution. 1H NMR (500 MHz, DMSO-d6) δ (ppm) 3.28-3.670 (br, 8H), 4.43 (s, 2H), 5.00 (s, 1H), 6.06 (s, 1H), 6.24 (d, J=8.2 Hz, 1H), 7.00 (s, 1H), 7.12-7.65 (m, 13H), 7.67 (d, J=8.8 Hz, 1H). 13C NMR (125 MHz, DMSO-d6): δ (ppm) 43.5, 46.0, 95.3, 102.7, 127.0, 127.3, 128.3, 128.4, 128.5, 128.6, 129.6, 132.4, 136.0, 139.3, 151.7, 154.2, 167.0, 168.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420640B2
Source datasetuspto-grants-2013_04
ORD IDord-9503ecd5c6b44a3eb6ce9a3e4225965e
Source noteuspto-grants-2013_04