HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903188Generated: November 2, 2026
Isobutyl chloroformate → 6-{3-[N-ethyl-N-(2-pyridyl)aminocarbonyl]propoxy}carbostyril
https://huagongshe.com/reaction/1903188
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 2-(Ethylamino)pyridine | HCID 11804745 | — |
| Reactant | 4-((2-Oxo-1,2-dihydroquinolin-6-yl)oxy)butanoic acid | HCID 12866342 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 6-{3-[N-ethyl-N-(2-pyridyl)aminocarbonyl]propoxy}carbostyril | HCID 12836955 | — |
Reaction Steps
Into 300 ml of chloroform were added 9.9 g of 6-(3-carboxypropoxy)carbostyril and 6.5 ml of DBU. The outside of the reaction vessel containing the abovementioned mixture was ice-cooled and 5.7 ml of isobutyl chloroformate was added dropwise under stirring condition. After the addition operation, stirring was continued for 1 hour at a room temperature and 5.4 g of 2-ethylaminopyridine was added dropwise, then the reaction was continued for 5 hours under stirring condition. The reaction mixture was washed with a diluted NaHCO3 aqueous solution and water, and was concentrated. The residue thus obtained was treated by a silica-gel column chromatography (solvent used was a mixture of chloroform:methanol=20:1) and the elute thus obtained was concentrated then was recrystallized from methanol, to obtain 4.5 g of 6-{3-[N-ethyl-N-(2-pyridyl)aminocarbonyl]propoxy}carbostyril in the form of colorless needle-like crystals. Melting point: 148°-149° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04435404 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-f80d78a5cf8646e9b40df407ed380c35 |
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| Source note | uspto-grants-1984_03 |
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