HuagongsheHuagongshe Chemistry Print Report · For research reference only
2H-[1,3]Dioxolo[4,5-b]pyridin-7-amine → HCID 68544982, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2H-[1,3]Dioxolo[4,5-b]pyridin-7-amine | HCID 45079475 | — |
| Reactant | 4-Chloro-7-(3-chloropropoxy)-6-methoxyquinazoline | HCID 57447227 | — |
| Product | HCID 68544982 | HCID 68544982 | 68% |
Reaction Steps
Using an analogous procedure to that described in Example 14, 4-chloro-7-(3-chloropropoxy)-6-methoxyquinazoline was reacted with 4-amino-2,3-methylenedioxypyridine to give the title compound in 68% yield; NMR Spectrum: (DMSOd6) 2.26 (m, 2H), 3.83 (m, 2H), 3.96 (s, 3H), 4.28 (m, 2H), 6.12 (s, 2H), 7.15 (br d, 1H), 7.25 (s, 1H), 7.61 (d, 1H), 7.81 (s, 1H), 8.49 (s, 1H), 9.79 (br s, 1H); Mass Spectrum: M+H+ 389.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07462623B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-06362361d9154e5c94f0071e89c665f4 |
| Source note | uspto-grants-2008_12 |