HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296060Generated: November 1, 2026
2-Methoxyacetohydrazide → 1-(methoxymethyl)-6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine
https://huagongshe.com/reaction/2296060
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methoxyacetohydrazide | HCID 2759532 | — |
| Reactant | 7-chloro-2-methylmercapto-5-phenyl-3H-1,4-benzodiazepine | HCID 12570858 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | 1-(methoxymethyl)-6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine | HCID 12560614 | — |
Reaction Steps
A solution of 10.0 g of 2-(methylthio)-5-phenyl-7-chloro-3H-1,4-benzodiazepine and 4.85 g of 2-methoxyacetic acid hydrazide (cp. E. J. Browne and J. B. Polya, J.Chem.Soc. 1962, 5149-5152) in 70 ml of abs. hexamethylphosphoric acid triamide is heaated for 11 hours at 140°. The solvent is then distilled off in vacuo. The residue is taken up in methylene chloride; the solution is washed with water and then with saturated sodium chloride solution, dried over sodium sulphate, and concentrated by evaporation. Crystallisation of the concentration residue from ethyl acetate/petroleum ether yields 1-(methoxymethyl)-6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine, M.P. 185°-191°. After chromatography of the mother liquor on 100 g of silica gel "Merck", a further amount of final product of the same melting point can be isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04427590 |
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| Source dataset | uspto-grants-1984_01 |
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| ORD ID | ord-7cf8edc254f34e37a1f26cc9a614afc5 |
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| Source note | uspto-grants-1984_01 |
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