HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethylamine → N-(4-benzyloxy-3-fluorophenyl)-N'-(2-phenylethyl)ethanediamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethylamine | HCID 1001 | — |
| Reactant | Ethyl 2-((4-(benzyloxy)-3-fluorophenyl)amino)-2-oxoacetate | HCID 57810427 | — |
| Product | N-(4-benzyloxy-3-fluorophenyl)-N'-(2-phenylethyl)ethanediamide | HCID 57810151 | 99% |
Reaction Steps
Phenethyl-amine (33 mL, 520 mmol) was added to ethyl [(4-benzyloxy-3-fluorophenyl)amino](oxo)acetate (81 g, 260 mmol) and the mixture was sonicated at room temperature for 30 min. The resulting solid was filtered, washed with water and dried to give N-(4-benzyloxy-3-fluorophenyl)-N′-(2-phenylethyl)ethanediamide (100 g, 99%). 1H NMR (400 MHz, d6-DMSO): δ 10.72 (br s, 1H), 9.05 (m, 1H), 8.78 (m, 1H), 7.77 (m, 1H), 7.59 (m, 1H), 7.46-7.19 (m, 8H), 5.16 (m, 2H), 3.45 (m, 2H), 2.83 (m, 2H); IR (cm−1): 2980, 2883, 1653, 1522, 1506, 1441, 1385, 1221, 1122, 951, 808, 746, 696, 584; LC/MS (M+H=393).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08067436B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-b31257133d934ec9b4318e3d6df3e534 |
| Source note | uspto-grants-2011_11 |