HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112249Generated: October 31, 2026
Dimethylformamide → Ethyl 7-Chloropyrimido[4,5-b]quinolin-4(3H)-one-2-carboxylate
https://huagongshe.com/reaction/1112249
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 12594648 | HCID 12594648 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 7-Chloropyrimido[4,5-b]quinolin-4(3H)-one-2-carboxylate | HCID 135705337 | — |
Reaction Steps
A mixture of 6-chloro-2-aminoquinoline-3-carboxamide (2.2 g., 0.01 mole), sodium hydride (0.52 g. 0.012 mole as 56% dispersion in oil) and N,N-dimethylformamide (20 ml.) is added to a solution of diethyl oxalate (5 ml.) and N,N-dimethylformamide (5 ml.). The reaction mixture is stirred for fifteen minutes, a second portion of sodium hydride (0.52 g., 0.012 mole) added and stirred continued for an additional 15 minutes. Acetic acid (25.0 ml.) is cautiously added to the mixture followed by water (50 ml.). The tan precipitate is removed by filtration and dried (2.0 g. of crude ester). It is purified by chromatography on silica gel using chloroform:2B ethanol (99:1) as eluant. The product, recovered by concentration of the eluate, is recrystallized from acetic acid. Yield = 1.3 g. (37.3%). M.P. 260.5° C. (dec.). Mass spectra gave m/e = 303.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04120962 |
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| Source dataset | uspto-grants-1978_10 |
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| ORD ID | ord-949570828a714a9fb3b476a36bc67bfe |
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| Source note | uspto-grants-1978_10 |
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