HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-chloro-2H-[1,3]dioxolo[4,5-b]pyridin-7-amine → HCID 68541592, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-chloro-2H-[1,3]dioxolo[4,5-b]pyridin-7-amine | HCID 68548651 | — |
| Reactant | HCID 85971021 | HCID 85971021 | — |
| Product | HCID 68541592 | HCID 68541592 | 86% |
Reaction Steps
Using an analogous procedure to that described in Example 1, 4-chloro-7-(2-chloroethoxy)-5-isopropoxyquinazoline was reacted with 4-amino-5-chloro-2,3-methylenedioxypyridine to give the title compound in 86% yield; NMR Spectrum: (CDCl3) 1.55 (d, 6H), 3.9 (t, 2H), 4.4 (t, 2H), 4.9 (m, 1H), 6.2 (s, 2H), 6.6 (s, 1H), 6.85 (s, 1H), 7.75 (s, 1H), 8.6 (s, 1H), 9.65 (s, 1H); Mass Spectrum: M+H+ 437 and 439.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07462623B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-fab532d4900842d2a1532762135b753d |
| Source note | uspto-grants-2008_12 |