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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 2-(Benzylamino)-4-(4-benzoylpiperazin-1-yl)benzoic acid | HCID 58425660 | — |
| Reactant | Methylamine tetrahydrofuran | HCID 66615946 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(benzylamino)-N-methyl-4-(4-benzoylpiperazin-1-yl)benzamide | HCID 67181886 | 36% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08420640B2 |
|---|
| Source dataset | uspto-grants-2013_04 |
|---|
| ORD ID | ord-b6a417b14e064bf998c826e6e45fc795 |
|---|
| Source note | uspto-grants-2013_04 |
|---|