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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844276Generated: October 31, 2026

Dibromomethane → 4-(2-(5-bromo-4-(7-methoxy-4-methylnaphthalen-1-yl)-4H-1,2,4-triazol-3-ylthio)acetamido)-3-chlorobenzoic acid

https://huagongshe.com/reaction/1844276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibromomethaneHCID 3024—
ReactantDichloroacetic AcidHCID 6597—
ReactantSodium NitriteHCID 23668193—
Reactant4-(2-(5-amino-4-(7-methoxy-4-methylnaphthalen-1-yl)-4H-1,2,4-triazol-3-ylthio)acetamido)-3-chlorobenzoic acidHCID 59813114—
CatalystBenzyltriethylammonium bromideHCID 165294—
Product4-(2-(5-bromo-4-(7-methoxy-4-methylnaphthalen-1-yl)-4H-1,2,4-triazol-3-ylthio)acetamido)-3-chlorobenzoic acidHCID 1605869724%

Reaction Steps

Dichloroacetic acid (0.1 mL, 1.2 mmol) was added to a mixture of compound 10 (304 mg, 0.6 mmol), benzyltriethyl ammonium bromide (492 mg, 1.8 mmol) and sodium nitrite (828 mg, 12 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 column chromatography (95% dichloromethane/5% methanol) to afford 80 mg, 24% yield of 4-(2-(5-bromo-4-(7-methoxy-4-methylnaphthalen-1-yl)-4H-1,2,4-triazol-3-ylthio)acetamido)-3-chlorobenzoic acid (11).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946273B2
Source datasetuspto-grants-2015_02
ORD IDord-aee459ba0bfe43099e2fd8e4f8037243
Source noteuspto-grants-2015_02