HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-methylsulfonyl-11H-s-triazolo[3,4-b][3]benzazapine → 3-methoxy-11H-s-triazolo[3,4-b][3]benzazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-methylsulfonyl-11H-s-triazolo[3,4-b][3]benzazapine | HCID 21323525 | — |
| Reactant | Sodium methanolate methanol | HCID 23694274 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-methoxy-11H-s-triazolo[3,4-b][3]benzazepine | HCID 21323368 | — |
Reaction Steps
To 0.522 g of 3-methylsulfonyl-11H-s-triazolo[3,4-b][3]benzazepine in 5 ml of methanol was added 3 ml of 2 N-sodium methoxide/methanol. The mixture was refluxed for 15 minutes and then the solvent was evaporated off. The residue was diluted with water and extracted with chloroform. The chloroform layer was washed with water and dried over Na2SO4. The solvent was then evaporated off and the residue was treated with isopropyl ether. By the above procedure was obtained 3-methoxy-11H-s-triazolo[3,4-b][3]benzazepine as crystals. Recrystallization from ethyl acetate-n-hexane yielded colorless prisms, melting point: 160°-161° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04150139 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-a9d49ac76bfe42409466037a002bccaa |
| Source note | uspto-grants-1979_04 |