HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26526Generated: October 29, 2026
3-bromo-11H-s-triazolo[3,4-b][3]benzazepine → 3-methoxy-11H-s-triazolo[3,4-b][3]benzazepine
https://huagongshe.com/reaction/26526
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-bromo-11H-s-triazolo[3,4-b][3]benzazepine | HCID 21323390 | — |
| 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 a solution of 0.262 g of 3-bromo-11H-s-triazolo [3,4-b][3]benzazepine in 2 ml of methanol was added 1.0 ml of 2 N-sodium methoxide/methanol and the mixture was refluxed for one hour. The solvent was evaporated off and, following the addition of water, the residue was extracted with ethyl acetate. The ethyl acetate 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: 161°-162° C. The infrared absorption spectrum of this product was identical with that of the compound obtained in Example 34.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04150139 |
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| Source dataset | uspto-grants-1979_04 |
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| ORD ID | ord-ce7514a5756e492dbd0762883753a63b |
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| Source note | uspto-grants-1979_04 |
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