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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616908Generated: October 31, 2026

Hydrochloric Acid → 9-chloro-2-methyl-7-phenyl-5H[1,2,4]triazolo-[5,1-a] [2,4]benzodiazepine

https://huagongshe.com/reaction/616908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexamethylenetetramineHCID 4101—
Reactant7-Chloro-2-methyl-5-phenyl-5H-[1,2,4]triazolo[5,1-a]isoindol-5-amineHCID 12468023—
Solvent1,2-DimethoxyethaneHCID 8071—
Product9-chloro-2-methyl-7-phenyl-5H[1,2,4]triazolo-[5,1-a] [2,4]benzodiazepineHCID 1246802540.5%

Reaction Steps

To a stirring solution of 3.1 g (10.4 mmol) of 7-chloro-2-methyl-5-phenyl-5H-[1,2,4]triazolo[5,1-a]-isoindol-5-amine and 3.1 g (22 mmol) of hexamethylenetetramine (hexamine) in 75 ml of DME is added 1.5 ml of 4 N HCl (dioxane). A precipitate forms immediately and the two phase mixture is refluxed. After 5 hours another 1.0 g of hexamine is added and reflux is continued overnight. An additional 1.5 ml of the HCl solution is added after 12 hours and again after an additional 24 hours. After another 24 hours, thin layer chromatography (TLC) shows the disappearance of starting material. The mixture is filtered and the solvent is removed from the filtrate under vacuum. The residue is taken up in CHCl3 and applied to a 5×10 cm silica gel column (Baker 60-200 mesh). The column is eluted with CHC13 until all of the high Rf material (followed by TLC) is recovered. The solvent is removed in vacuo and the residue recrystallized from 20 ml of acetonitrile to yield 1.3 g of pure product: m.p. 150.5°-152° [concentration of the mother liquor gives an additional 0.2 g for a total yield of 1.5 g (46.6%)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04076823
Source datasetuspto-grants-1978_02
ORD IDord-b362991737ce4fbcbb7df3a5a34cb890
Source noteuspto-grants-1978_02