HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 5-Azaacetanthranil
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 3-Aminopicolinic acid | HCID 73836 | — |
| Product | 5-Azaacetanthranil | HCID 12204217 | — |
Reaction Steps
Imidazo[4,5-c][1,5]naphthyridine-2,4-diamines of the invention can be prepared according to Reaction Scheme V, wherein D, R, R1, R4a, Ph, m, and p are as defined above. 3-Aminopyridine-2-carboxylic acids of Formula XXXIII are known and can be prepared by known methods. The compound where n and m are both 0 is commercially available. In step (1) of Reaction Scheme V, a 3-aminopyridine-2-carboxylic acid of Formula III is heated with acetic anhydride to provide a 2-methyl-4H-pyrido[3,2-d][1,3]oxazin-4-one of Formula XXXIV.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143270B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-9b3b22b2ecd04bc9b4df3ec658b5d902 |
| Source note | uspto-grants-2012_03 |