HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414905Generated: October 25, 2026
Ammonia → 6-phenyl-8-chloro-4H-s-triazolo [4,3-a][1,4]benzodiazepine-1-carboxamide
https://huagongshe.com/reaction/1414905
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxaldehyde | HCID 21486011 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 6-phenyl-8-chloro-4H-s-triazolo [4,3-a][1,4]benzodiazepine-1-carboxamide | HCID 21486018 | — |
Reaction Steps
0.245 g (0.005 mole) of sodium cyanide is added at 0°, with stirring, to the saturated solution of ammonia in 15 ml of isopropanol. After 5 minutes, a solution of 0.322 g (0.001 mole) of 6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxaldehyde in ca. 10 ml of isopropanol is added together with 0.87 g of manganese dioxide. After a further 10 minutes, another addition is made of 0.87 g (total 0.02 mole) of manganese dioxide, and the mixture stirred for 4 hours at 0°. After the addition of ca. 40 ml of methylene chloride, the reaction mixture is filtered and the filtrate concentrated by evaporation. Crystallisation of the residue from methanol/ethyl acetate/petroleum ether yields 6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine-1-carboxamide, M.P. 285°-289°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04002764 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-0e7597d4961c4450a9ef7f4f5254d266 |
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| Source note | uspto-grants-1977_01 |
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