HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Diphenylmethyl)-4-piperidinamine → HCID 54099729, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Diphenylmethyl)-4-piperidinamine | HCID 12875535 | — |
| Reactant | 2-(Heptylamino)-4H-3,1-benzoxazin-4-one | HCID 54169928 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 54099729 | HCID 54099729 | 43.7% |
Reaction Steps
A mixture of 2-n-heptylamino-4H-3,1-benzoxazin-4-one (3.0 g, 10 mmol) and 4-amino-1-diphenylmethylpiperidine (3.0 g, 10 mmol) in toluene (20 ml) was refluxed for 3 hours and then concentrated. The residue was purified by column chromatography on silica gel (20% ethyl acetate in hexane) to give 2-(N'-n-heptylureido)-N-(1-diphenylmethylpiperidin-4-yl)benzamide (2.3 g, 40%): mp 182° C.; 1H NMR (CDCl3)ppm: 0.87 (3H, t), 1.27-1.30 (8H, m), 1.47-1.67 (4H, m), 1.95-2.12 (4H, m), 2.84 (2H, d), 3.24 (2H, q), 3.90-3.94 (1H, m), 4.26 (1H, s), 4.56 (1H, t), 6.09 (1H, d), 6.92-6.98 (1H, m), 7.16-7.44 (12H, m), 8.41 (1H, d), 10.26 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05872115 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-2c14145ba42843beb0d5825dc1f78cef |
| Source note | uspto-grants-1999_02 |