HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164950Generated: October 29, 2026
Triethylamine → 2,N-Dimethyl-N-(3-methyl-4-nitrophenyl)pyridine-4-carboxamide
https://huagongshe.com/reaction/1164950
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Methyl-4-pyridinecarbonyl chloride | HCID 11788423 | — |
| Reactant | N,3-Dimethyl-4-nitroaniline | HCID 14146034 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,N-Dimethyl-N-(3-methyl-4-nitrophenyl)pyridine-4-carboxamide | HCID 19863463 | — |
Reaction Steps
To a solution of 16.6 g (0.1 mol) of 3,N-dimethyl-4-nitrobenzenamine and 10.2 g (0.1 mol) of triethylamine in mL of methylene chloride cooled to 0° C. under a nitrogen atmosphere add slowly a solution of 15.6 g (0.1 mol) of 2-methylpyridine-4-carbonyl chloride (prepared from the corresponding acid and thionyl chloride) such that the temperature is maintained between 0°-5° C. After the addition is complete, stir the mixture for 6 h and allow to warm slowly to room temperature. Quench the reaction mixture by the addition of 50 mL of water. Separate the layers and wash the organic layer with two 50 mL portions of water, two 50 mL portions of 5% sodium bicarbonate solution and 50 mL of saturated sodium chloride solution. Dry the methylene chloride solution over anhydrous sodium sulfate. Remove the drying agent by filtration and evaporate the solvent to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04906634 |
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| Source dataset | uspto-grants-1990_03 |
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| ORD ID | ord-9e770a796a1a40d183e65ca7df663776 |
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| Source note | uspto-grants-1990_03 |
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