HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354888Generated: October 25, 2026
Diphenyl Ether → methyl 4-oxo-10-(2-ethylbutyramido)-4H-pyrimido[1,2-C]quinazoline-3-carboxylate
https://huagongshe.com/reaction/354888
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diphenyl Ether | HCID 7583 | — |
| Reactant | Dimethyl[[6-(2-ethylbutyramido)-4-quinazolinylamino]methylene]propanedioate | HCID 13060503 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | methyl 4-oxo-10-(2-ethylbutyramido)-4H-pyrimido[1,2-C]quinazoline-3-carboxylate | HCID 13060555 | 78.1% |
Reaction Steps
A mixture of dimethyl[[6-(2-ethylbutyramido)-4-quinazolinylamino]methylene]propanedioate (5.3 g) and diphenyl ether (32 ml) was heated at 255° C. for 15 minutes and cooled to ambient temperature. Hexane was added to the reaction mixture. The resulting crystals were filtered off, washed with hexane and dried. The crude crystals were dissolved in a mixture of chloroform and methanol (10:1) under heating. Insoluble materials were removed by filtration. The filtrate was concentrated under reduced pressure to give crystals, which were recrystallized from a mixture of chloroform and hexane to give methyl 4-oxo-10-(2-ethylbutyramido)-4H-pyrimido[1,2-C]quinazoline-3-carboxylate (3.81 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04377580 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-c2457fe689d94c68b6796249a04d2da1 |
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| Source note | uspto-grants-1983_03 |
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