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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235499Generated: October 31, 2026

2,4,6-Trimethylbenzoyl chloride → 2,4,6-Trimethyl-N-(7-nitro-1,3-benzothiazol-2-yl)benzamide

https://huagongshe.com/reaction/2235499

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-Trimethylbenzoyl chlorideHCID 97038—
Reactant7-Nitro-1,3-benzothiazol-2-amineHCID 4325724—
SolventPyridineHCID 1049—
Product2,4,6-Trimethyl-N-(7-nitro-1,3-benzothiazol-2-yl)benzamideHCID 8604920266%

Reaction Conditions

Temperature75 °C

Reaction Steps

To 0.089 g (0.46 mmol) of 7-nitro-1,3-benzothiazol-2-amine in 1 mL of pyridine was added 0.17 g (0.91 mmol) of 2,4,6-trimethylbenzoyl chloride. The mixture was heated to 75° C. for 18 h and the volatiles were removed in vacuo. The residue was washed with water and 1 N hydrochloric acid, dissolved in ethyl acetate, dried over sodium sulfate, filtered, concentrated in vacuo and the resulting crude solid was purified by flash chromatography eluting with 25% ethyl acetate/hexanes mixture to give 0.103 g (66%) of the title compound as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714009B2
Source datasetuspto-grants-2010_05
ORD IDord-3a18adc1c6664865b192f20b25dfca42
Source noteuspto-grants-2010_05