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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15025Generated: October 25, 2026

4-Methyl-3-nitrobenzoyl chloride → 6-(4-Methyl-3-nitrophenyl)-3-(3,4,5-trimethoxyphenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole

https://huagongshe.com/reaction/15025

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-3-nitrobenzoyl chlorideHCID 66323—
ReactantHCID 178488244HCID 178488244—
SolventPhosphorus oxychlorideHCID 24813—
Product6-(4-Methyl-3-nitrophenyl)-3-(3,4,5-trimethoxyphenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazoleHCID 2495487187.9%

Reaction Steps

A mixture of 4-amino-3-mercapto-5-(3,4,5-trimethoxyphenyl)-4H-1,2,4-triazole (220 mg, 0.78 mmol) and 4-methyl-3-nitrobenzoyl chloride (156 mg, 0.78 mmol) in phosphoryl chloride (2 mL) was refluxed for 3 h. The solvent was evaporated and the residue was dissolved in dichloromethane (20 mL). It was neutralized by aqueous sodium carbonate. The organic layer was dried over sodium sulfate, and concentrated to give 293 mg (85%) of the title compound as solid. 1H NMR (CDCl3): 8.59 (d, J=2.1 Hz, 1H), 8.05-8.01 (dd, J=7.8, 1.8 Hz, 1H), 7.73 (s, 1H), 7.62 (d, J=8.1 Hz, 1H), 4.02 (s, 6H), 3.95 (s, 3H), 2.75 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732468B2
Source datasetuspto-grants-2010_06
ORD IDord-321f1925f9ae4c01af76f2f17cfae4fa
Source noteuspto-grants-2010_06