HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Heptanamine → HCID 53946422, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Heptanamine | HCID 8127 | — |
| Reactant | HCID 53852154 | HCID 53852154 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 53946422 | HCID 53946422 | 95% |
Reaction Steps
A solution of 2-phenoxycarbonylamino-N-(1-phenoxylcarbonylpiperidin-4-yl)benzamide (1.6 g, 3.5 mmol) and n-heptylamine (0.45 g, 3.9 mmol) in toluene (20 ml) was refluxed for 4 hours and then concentrated. The residue was purified by column chromatography on silica gel (50% ethyl acetate in petroleum ether) to give 2-(N'-n-heptylureido)-N-(1-phenoxy carbonylpiperidin-4-yl)benzamide: yield 95.0%: mp 142°-144° C.; 1H NMR (CDCl3)ppm: 0.88 (3H, t) 1.28-1.33 (7H, m), 19-1.62 (4H, m), 2.05-2.17 (2H, m), 3.04-3.19 (2H, m), 3.25 (2H, q), 4.10-4.15 (1H, m), 4.24-4.40 (2H, m), 4.59 (1H, t), 6.35 (1H, d), 6.92 (1H, t), 6.97-7.44 (8H, m), 8.40 (1H,d), 10.20 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05872115 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-0c4ad84f1a194235b310a9654cfd65f4 |
| Source note | uspto-grants-1999_02 |