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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764531Generated: October 31, 2026

Sulfuric Acid → 6-phenyl-4H-s-triazolo[4,3-a][1,4-]benzodiazepine

https://huagongshe.com/reaction/1764531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium BicarbonateHCID 516892—
Reactant2-hydrazino-5-phenyl-3H-1,4-benzodiazepineHCID 12612389—
ReactantEthylorthoformateHCID 53630039—
SolventEthanolHCID 702—
Product6-phenyl-4H-s-triazolo[4,3-a][1,4-]benzodiazepineHCID 12562518—

Reaction Steps

To a mixture of 1 part of 2-hydrazino-5-phenyl-3H-1,4-benzodiazepine, prepared in Example 3, 2 parts by volume of ethyl orthoformate and 20 parts by volume of ethanol, 0.44 part by volume of concentrated sulfuric acid is added dropwise with ice-cooling. The mixture is stirred at room temperature for 30 minutes and neutralized with saturated aqueous sodium bicarbonate. The resulting oily substance is extracted with methylene chloride. The methylene chloride layer is washed with water, dried over sodium sulfate and the solvent is evaporated, whereby 6-phenyl-4H-s-triazolo [4,3-a] [1,4] benzodiazepine is yielded as crystals. Recrystallization from a mixture of acetone and n-hexane yields colorless needles melting at 195° C to 196° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04116956
Source datasetuspto-grants-1978_09
ORD IDord-d75dd46618774ce4b021bb57bed51574
Source noteuspto-grants-1978_09