HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethylamine → 6-(1-Phenethylamino-indan-5-yloxy)-nicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethylamine | HCID 1001 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 6-(1-Oxo-indan-5-yloxy)-nicotinamide | HCID 59750639 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Product | 6-(1-Phenethylamino-indan-5-yloxy)-nicotinamide | HCID 11773191 | 87.8% |
Reaction Steps
Using a method similar to Example 14, using 6-(1-oxo-indan-5-yloxy)-nicotinamide (Intermediate 4, 805 mg, 3.00 mmol), phenethylamine (436 mg, 3.60 mmol), Ti(iPrO)4 (1.70 g, 6.00 mmol), TiCl4 (1.0M/DCM, 6.00 ml, 6.00 mmol), and NaBH3CN (377 mg, 6.00 mmol) gives the title compound (984 mg) as a light yellow solid. Mass spectrum (ion spray): m/z=374 (M+1); 1HNMR (CDCl3): 8.59 (s, 1H), 8.15 (d, 1H), 7.33-7.19 (m, 6H), 6.98 (s, 1H), 6.95-6.91 (m, 2H), 5.99 (br. s, 2H), 4.26 (t, 1H), 3.04-2.94 (m, 3H), 2.88-2.74 (m, 3H), 2.44 (m, 1H), 1.84 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07399774B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-3c124f27fbab40e98df1c26413c80da9 |
| Source note | uspto-grants-2008_07 |