HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-Acetylamino-8-methoxy-4-phenylimino-4H-1,3,5-triazino[2,1-b]benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Amino-8-methoxy-4-phenylimino-4H-1,3,5-triazino[2,1-b]benzothiazole | HCID 20428309 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-Acetylamino-8-methoxy-4-phenylimino-4H-1,3,5-triazino[2,1-b]benzothiazole | HCID 135797546 | 79.6% |
Reaction Steps
2-Amino-8-methoxy-4-phenylimino-4H-1,3,5-triazino[2,1-b]benzothiazole (0.3 g) and acetic anhydride (0.14 g) in dry pyridine (15 mls) were heated at 100° for 24 hours. After cooling to room temperature, methanol (5 mls) was added, the solution was stirred for 1 hour and the solvents were removed in vacuo. The residue was dissolved in chloroform, the solution washed with water, brine, dried (Na2SO4) and evaporated in vacuo to give a yellow solid (0.27 g). Purification by chromatography (silica gel, chloroform) gave the title compound as pale yellow crystals (0.18 g), mp 248°-29°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04499269 |
| Source dataset | uspto-grants-1985_02 |
| ORD ID | ord-4c398afa0cc54205829a80cbce2b62ff |
| Source note | uspto-grants-1985_02 |