HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 2H-[1,3]Dioxolo[4,5-b]pyridin-7-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 68546563 | HCID 68546563 | — |
| Product | 2H-[1,3]Dioxolo[4,5-b]pyridin-7-amine | HCID 45079475 | 80% |
Reaction Steps
Using an analogous procedure to that described in the last paragraph of that portion of Example 1 that is concerned with the preparation of starting materials, tert-butyl 2,3-methylenedioxypyrid-4-ylcarbamate was reacted with trifluoroacetic acid to give 4-amino-2,3-methylenedioxypyridine in 80% yield; NMR Spectrum: (CDCl3) 3.98 (m, 2H), 5.98 (s, 2H), 6.24 (d, 1H), 7.44 (d, 1H); Mass Spectrum: M+H+ 139.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07462623B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-1cad3155649149cba66ca932f0d6967c |
| Source note | uspto-grants-2008_12 |