HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminopyridine → HCID 54717105, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | HCID 54719505 | HCID 54719505 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 54717105 | HCID 54717105 | — |
Reaction Steps
3.54 g. of 6-bromo-4-hydroxy-2-methyl-3-methoxycarbonyl-2H-thieno[2,3-e]-1,2-thiazine-1,1-dioxide are boiled under reflux for 6 hours with 1.42 g. of 2-aminopyridine in 150 ml. of absolute xylene. The reaction mixture is allowed to cool to room temperature. The precipitated crude product is recrystallized from dioxane and 6-bromo-4-hydroxy-2-methyl-3-(2-pyridylcarbamyol)-2H-thieno[2,3-e]-1,2-thiazine-1,1-dioxide having a melting point of 232°-235° is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04180662 |
| Source dataset | uspto-grants-1979_12 |
| ORD ID | ord-892dfbd038bb47e8b85a1c66eaa0e809 |
| Source note | uspto-grants-1979_12 |