HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604598Generated: October 30, 2026
Butanoic acid, 4-chloro-4-oxo-, methyl ester → 8-[2,6-Dichloro-3-(3-methoxycarbonylpropionylamino)benzyloxy]-2-methylquinoline
https://huagongshe.com/reaction/1604598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butanoic acid, 4-chloro-4-oxo-, methyl ester | HCID 73888 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 8-(3-Amino-2,6-dichlorobenzyloxy)-2-methylquinoline | HCID 10806520 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 8-[2,6-Dichloro-3-(3-methoxycarbonylpropionylamino)benzyloxy]-2-methylquinoline | HCID 19603299 | — |
Reaction Steps
To a mixture of 8-(3-amino-2,6-dichlorobenzyloxy)-2-methylquinoline (1.67 g), triethylamine (0.9 ml) and anhydrous dichloromethane (84 ml) was added 3-methoxycarbonylpropionyl chloride (0.7 ml). After stirring at ambient temperature for 9 hours, triethylamine (1.8 ml) and 3-methoxycarbonylpropionyl chloride (1.4 ml) were added thereto and the mixture was stirred for additional 30 minutes. The reaction mixture was washedwith water and saturated aqueous solution of sodium hydrogen carbonate, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by a silica gel column chromatography eluted with chloroform to give 8-[2,6-dichloro-3-(3-methoxycarbonylpropionylamino)benzyloxy]-2-methylquinoline (2.04 g) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05994368 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-3bc2f154716b48588c8f7a6a18d0dd58 |
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| Source note | uspto-grants-1999_11 |
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