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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108338Generated: October 30, 2026

Hydrochloric Acid → 10-Bromo-5H-benzo[f][1,2,4]triazolo[1,5-d][1,4]diazepin-6(7H)-one

https://huagongshe.com/reaction/2108338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChloroacetyl chlorideHCID 6577—
ReactantSodium HydroxideHCID 14798—
Reactant4-Bromo-2-(1H-1,2,4-triazol-3-yl)anilineHCID 62072644—
SolventPyridineHCID 1049—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
Product10-Bromo-5H-benzo[f][1,2,4]triazolo[1,5-d][1,4]diazepin-6(7H)-oneHCID 13633518346%

Reaction Conditions

Temperature11 °C

Reaction Steps

A solution of 4-bromo-2-(2H-[1,2,4]triazol-3-yl)-phenylamine (25.0 g, 105 mmol) in dioxane (870 mL) and pyridine (10.0 mL) was cooled to 12° C. A solution of chloroacetyl chloride (9.56 mL, 121 mmol) in diethylether (34.7 mL) was added dropwise over a period of 8 min. The mixture was stirred at 10-12° C. for 75 min and treated within 5 min with aq NaOH 2N (126 mL, 251 mmol). The mixture was stirred for 17.5 h at ambient temperature. The pH thereby dropped to about pH=9 and it was adjusted to pH=8 with 3N HCl (6 mL). After evaporation the residue was stirred at 15° C. for 30 min in water (650 mL) and ethyl acetate (22 mL). The crystals were filtered off, washed with cold water and dried in vacuo. Trituration in ethyl acetate (100 mL) afforded the title compound (13.4 g, 46%) as a light yellow solid. MS: m/e=279.0/281.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514426B2
Source datasetuspto-grants-2009_04
ORD IDord-c5e1387351b5419999052991a6062f92
Source noteuspto-grants-2009_04