Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066407Generated: November 1, 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/2066407

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 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° C.-12° C. for 75 min and treated within 5 min with aqueous NaOH (2 N, 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 HCl (3 N, 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 numberUS08293730B2
Source datasetuspto-grants-2012_10
ORD IDord-dbee5828f0bc4541b1512d08e51aedf8
Source noteuspto-grants-2012_10