HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Amino-2-(2-phenylchroman-6-yloxy)pyridine → 6-[2-(2-Fluorophenyl)chroman-6-yloxy]-pyridin-3-ylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Amino-2-(2-phenylchroman-6-yloxy)pyridine | HCID 17978478 | — |
| Reactant | 2-[2-(2-Fluorophenyl)chroman-6-yloxy]-5-nitropyridine | HCID 17978646 | — |
| Product | 6-[2-(2-Fluorophenyl)chroman-6-yloxy]-pyridin-3-ylamine | HCID 17978503 | — |
Reaction Steps
6-[2-(2-Fluorophenyl)chroman-6-yloxy]-pyridin-3-ylamine was prepared as described for 5-amino-2-(2-phenylchroman-6-yloxy)pyridine in Example 26 starting from 240 mg of 2-[2-(2-fluorophenyl)chroman-6-yloxy]-5-nitropyridine (Example 19(d)). 1H NMR (400 MHz, d6-DMSO) δ: 7.52 (m, 1H), 7.51 (d, 1H, J 3.0 Hz), 7.41 (m, 1H), 7.28-7.24 (m, 2H), 7.05 (dd, 1H, J 8.6, 3.0 Hz), 6.81-6.73 (m, 3H), 6.70 (d, 1H, J 8.6 Hz), 5.31 (dd, 1H, J 10.3, 2.2 Hz), 5.00 (s, 2H), 2.98 (m, 1H), 2.72 (m, 1H), 2.15 (m, 1H), 2.06 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07425568B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-1c1b91bf6edd4daaa0e6839db28f3959 |
| Source note | uspto-grants-2008_09 |