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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | Ethanol, reaction products with ammonia, distn. residues | HCID 22020343 | — |
| Reactant | 2-(Benzylamino)-4-(4-benzoylpiperazin-1-yl)benzoic acid | HCID 58425660 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 46200788 | HCID 46200788 | 48.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08420640B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-9503ecd5c6b44a3eb6ce9a3e4225965e |
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| Source note | uspto-grants-2013_04 |
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