HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239912Generated: October 26, 2026
Diisopropylethylamine → Ethyl 4-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-3,5-dimethyl-benzoate
https://huagongshe.com/reaction/239912
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Propylphosphonic anhydride | HCID 111923 | — |
| Reactant | Benzoic acid, 4-amino-3,5-dimethyl-, ethyl ester | HCID 201013 | — |
| Reactant | 6-Chloro-3-methylpyridine-2-carboxylic acid | HCID 46941470 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 4-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-3,5-dimethyl-benzoate | HCID 86707305 | 57.5% |
Reaction Steps
To a solution of 6-chloro-3-methyl-pyridine-2-carboxylic acid (0.78 g, 4.55 mmol) in CH2Cl2 (15 mL) at room temperature are added ethyl 4-amino-3,5-dimethyl-benzoate (0.878 g, 4.55 mmol) and N,N-diisopropylethylamine (1.98 ml, 11.36 mmol). After stirring the reaction mixture for 10 minutes, 1-propanephosphonic acid cyclic anhydride (50% solution in ethyl acetate, 3.25 ml, 5.46 mmol) is added via syringe. After 48 hours, the solvent is removed under reduced pressure and the residue is diluted with water and extracted with ethyl acetate. The organic layers are combined and dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The resulting residue is purified by flash chromatography (silica gel) using a gradient of 0-40% ethyl acetate in hexanes. After purification, the solid is triturated with 30% ethyl acetate in hexanes and filtered to give the title compound as a white powder (0.907 g, 57.5%). Mass spectrum (m/z): 347.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642768B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-9fa3c5cd6f834b8fb1880df9095e743b |
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| Source note | uspto-grants-2014_02 |
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