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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448148Generated: October 25, 2026

Dibromomethane → 4-(2-(5-bromo-4-(2-chloro-4-cyclopropyl-6-methylphenyl)-4H-1,2,4-triazol-3-ylthio)acetamido)-3-chlorobenzoic acid

https://huagongshe.com/reaction/448148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibromomethaneHCID 3024—
ReactantDichloromethaneHCID 6344—
ReactantDichloroacetic AcidHCID 6597—
ReactantSodium NitriteHCID 23668193—
Reactant4-(2-(5-amino-4-(2-chloro-4-cyclopropyl-6-methylphenyl)-4H-1,2,4-triazol-3-ylthio)acetamido)-3-chlorobenzoic acidHCID 59813099—
CatalystBenzyltriethylammonium bromideHCID 165294—
Product4-(2-(5-bromo-4-(2-chloro-4-cyclopropyl-6-methylphenyl)-4H-1,2,4-triazol-3-ylthio)acetamido)-3-chlorobenzoic acidHCID 1622181542%

Reaction Steps

Dichloroacetic acid (0.065 mL, 0.78 mmol) was added to a mixture of compound 6 (192 mg, 0.39 mmol), benzyltriethyl ammonium bromide (318 mg, 1.17 mmol) and sodium nitrite (538 mg, 7.8 mmol) in dibromomethane (10 mL). The mixture was stirred at room temperature for 18 hours in the dark. The reaction mixture was then concentrated and the resulting residue was purified by prep. TLC (95% dichloromethane/5% methanol) to afford 88 mg, 42% yield of 4-(2-(5-bromo-4-(2-chloro-4-cyclopropyl-6-methylphenyl)-4H-1,2,4-triazol-3-ylthio)acetamido)-3-chlorobenzoic acid (7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481581B2
Source datasetuspto-grants-2013_07
ORD IDord-eae7be41017a4e9c8e131a947692d43f
Source noteuspto-grants-2013_07