HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl p-toluenesulfonate → HCID 22266863, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl p-toluenesulfonate | HCID 6645 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 22266814 | HCID 22266814 | — |
| Reactant | 8-Methoxyquinolin-2-amine | HCID 22266820 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 22266863 | HCID 22266863 | — |
| Product | HCID 178488368 | HCID 178488368 | — |
Reaction Steps
2-Amino-3-hydroxy-8-methoxyquinoline is prepared according to M. Y. Chu-Moyer (as above) starting from 2-amino-8-methoxyquinoline. This compound is treated with 3 equivalents of acetic anhydride in pyridine, and the reaction mixture is heated from room temperature to 120° C. and stirred overnight. The 2-methyl-5-methoxyoxazolo[4,5-b]quinoline thus generated is then heated with 3 equivalents of methyl tosylate at 70° C. for 8 hours to give the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820824B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-61abb1e3c4dd4db2a61f968bb0d8fd51 |
| Source note | uspto-grants-2010_10 |