HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595482Generated: October 25, 2026
4-Methylmorpholine → Ethyl 2-(6-chloro-4-(isopropylamino)nicotinamido)-3-oxobutanoate
https://huagongshe.com/reaction/595482
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Ethyl 2-amino-3-oxobutanoate | HCID 13282896 | — |
| Reactant | Ethyl 6-chloro-4-(cyclobutylamino)nicotinate | HCID 89689654 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 2-(6-chloro-4-(isopropylamino)nicotinamido)-3-oxobutanoate | HCID 89689546 | — |
Reaction Steps
A stirred solution of 6-chloro-4-(isopropylamino)nicotinic acid (2) in DCM (15 mL) was cooled to 0° C., oxalyl chloride (2 equiv) was added, followed by addition of 2 drops of DMF. The reaction mixture was stirred at room temperature for 2 h. The reaction mixture was concentrated to remove excess of oxalyl chloride. The acyl chloride, generated in-situ was dissolved in THF and added dropwise to a cool, stirred solution of ethyl 2-amino-3-oxobutanoate (1.1 equiv.) and NMM (5 equiv.) in THF. The reaction temperature was slowly brought to room temperature and stirred overnight. The reaction mixture was diluted with EtOAc and washed with water, followed by brine solution. The EtOAc layer was collected, dried over Na2SO4, filtered and concentrated. The crude material obtained was purified by column chromatography through silica gel and EtOAc:Pet. Ether as eluent to afford the title compound, ethyl 2-(6-chloro-4-(isopropylamino)nicotinamido)-3-oxobutanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242976B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-7a6d10f697a7416b9ad9f3f630ed45d2 |
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| Source note | uspto-grants-2016_01 |
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