HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783906Generated: October 29, 2026
1,2-Ethanediamine, N1,N1-bis(1-methylethyl)- → HCID 39468342, compound
https://huagongshe.com/reaction/1783906
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Ethanediamine, N1,N1-bis(1-methylethyl)- | HCID 8459 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 23689970 | HCID 23689970 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 39468342 | HCID 39468342 | 74% |
Reaction Steps
A suspension of 1.1 g (5 mmol) potassium 5-methoxycarbonyl-pyridine-2-carboxylate, 0.9 ml (12 mmol) thionyl chloride and 0.1 ml DMF in 5 ml dichloroethane was heated at reflux for 2 h. To the reaction mixture 5 ml CH2Cl2 were added and the solvent was evaporated. This procedure was repeated three times. The residue was suspended in 5 ml CH2Cl2 and a solution of 9.95 ml (5.5 mmol) 2-diisopropylaminoethylamine, 0.97 ml (7 mmol) triethylamine, 0.1 ml DMF in 5 ml CH2Cl2 was added under ice-cooling. After stirring for 12 h at rt the organic phase was extracted with water, 5% citric acid and aqueous NaHCO3 and dried over magnesium sulfate. After evaporation of the solvent the residue was subjected to silica gel chromatography (20% MeOH and 1% triethylamine in ethyl acetate) to yield 1.15 g (3.7 mmol) 6-(2-diisopropylamino-ethylcarbamoyl)-nicotinic acid methyl ester; exact MW [M+H] calcd: 308.20; MW found [M+H]: 308.20.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07501451B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-555416858ee142e9b821a504eebd6180 |
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| Source note | uspto-grants-2009_03 |
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