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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237130Generated: October 30, 2026

HCID 13078264, compound → HCID 21315212, compound

https://huagongshe.com/reaction/237130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13078264HCID 13078264—
ReactantAcetic Acid Mixture with Hydrobromic AcidHCID 21893785—
SolventDiethyl EtherHCID 3283—
ProductHCID 21315212HCID 21315212—

Reaction Steps

A mixture of 2',5-dichloro-2-(3-dimethylcarbamoyl-5-carbobenzoxyaminomethyl-1,2,4-triazol- 1-yl)benzophenone (3.6 g) and 30% hydrogen bromide-acetic acid (9 ml) is stirred at room temperature for 2 hours. The reaction mixture is mixed with ether, and the precipitate is isolated by decantation and washed thrice with ether, whereby 2',5-dichloro-2-(3-dimethylcarbamoyl-5-aminomethyl-1,2,4-triazol- 1-yl)-benzophenone hydrobromide is obtained. This hydrobromide (1.2 g) is added to a solution of chloroacetyl chloride (1.2 g) in benzene (40 ml) to give a solution, which is mixed with dimethylformamide (20 ml). The resultant mixture is stirred at room temperature for 3 hours. The reaction mixture is mixed with ethyl acetate and neutralized with aqueous sodium bicarbonate. The organic layer is separated, washed with water, dried, and evaporated under reduced pressure to remove the solvent. The residue is treated with ethanol/n-hexane to give 2',5-dichloro-2-[3-dimethylcarbamoyl-5-(2-chloroacetylamino)methyl-1,2,4-triazol- 1-yl]-benzophenone (12.9 g), which is recrystallized from ethyl acetate to give colorless needles melting at 80°-82° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04159374
Source datasetuspto-grants-1979_06
ORD IDord-a232e55b26fe4becaa0095f7fab4db07
Source noteuspto-grants-1979_06