HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Amino-2-(2-phenylchroman-6-yloxy)pyridine → 6-[2-(2-Aminophenyl)chroman-6-yloxy]-pyridin-3-ylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Amino-2-(2-phenylchroman-6-yloxy)pyridine | HCID 17978478 | — |
| Reactant | 5-Nitro-2-[2-(2-nitrophenyl)chroman-6-yloxy]pyridine | HCID 17978562 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Product | 6-[2-(2-Aminophenyl)chroman-6-yloxy]-pyridin-3-ylamine | HCID 17978457 | — |
Reaction Steps
6-[2-(2-Aminophenyl)chroman-6-yloxy]-pyridin-3-ylamine was prepared as described for 5-amino-2-(2-phenylchroman-6-yloxy)pyridine in Example 26 using 100 mg 5-nitro-2-[2-(2-nitrophenyl)chroman-6-yloxy]pyridine (Example 89(d)) and 700 mg of Zn. 1H NMR (300 MHz, d6-DMSO) δ: 7.51 (d, 1H, J 2.9 Hz), 7.15-7.18 (m, 1H), 7.05 (dd, 1H, J 8.6, 2.9 Hz), 6.98-7.00 (m, 1H), 6.77 (d, 1H, J 8.6 Hz), 6.73-6.75 (m, 2H), 6.66-6.71 (m, 2H), 6.56-6.61 (m, 1H), 5.11 (dd, 1H, J 10.4, 2.0 Hz), 5.01 (s, 2H), 4.99 (s, 2H), 2.94-2.99 (m, 1H), 2.66-2.74 (m, 1H), 2.06-2.13 (m, 1H), 1.88-1.95 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07425568B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-d8349279b39d474eae09bd8e894b1d1d |
| Source note | uspto-grants-2008_09 |