HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethylamine → HCID 11349721, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethylamine | HCID 1001 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 59750675 | HCID 59750675 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Product | HCID 11349721 | HCID 11349721 | 81.7% |
Reaction Steps
Using a method similar to Example 14, using 6-(4-methyl-1-oxo-indan-5-yloxy)-nicotinamide (Intermediate 12, 100 mg, 0.354 mmol), phenethylamine (52 mg, 0.425 mmol), Ti(iPrO)4 (201 mg, 0.708 mmol), TiCl4 (11.0M/DCM, 0.708 ml, 0.708 mmol), and NaBH3CN (44 mg, 0.708 mmol) gives the title compound (112 mg) as a white solid. Mass spectrum (ion spray): m/z=388 (M+1); 1HNMR (CDCl3): 8.57 (s, 1H), 8.14 (d, 1H), 7.32-7.19 (m, 5H), 7.14 (d, 1H), 6.91-6.87 (m, 2H), 6.03 (br. s, 2H), 428 (t, 1H), 3.01 (t, 2H), 2.94 (m, 1H), 2.85 (m, 2H), 2.74 (m, 1H), 2.44 (m, 1H), 2.02 (s, 3H), 1.86 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08101638B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-2759e68f269a4a91b101e671e034eb99 |
| Source note | uspto-grants-2012_01 |