HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270245Generated: October 31, 2026
Iodoethane → 3-Benzyloxy-1-ethyl-5,6,8-trifluoro-7-pyrrolidin-1-yl-1H-quinazoline-2,4-dione
https://huagongshe.com/reaction/2270245
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 3-Benzyloxy-5,6,7,8-tetrafluoro-1H-quinazoline-2,4-dione | HCID 22632880 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 3-Benzyloxy-1-ethyl-5,6,8-trifluoro-7-pyrrolidin-1-yl-1H-quinazoline-2,4-dione | HCID 22632997 | 22.1% |
Reaction Steps
A solution of 3-benzyloxy-5,6,7,8-tetrafluoro-1H-quinazoline-2,4-dione (Example W-3, 0.90 g, 2.7 mmol), in DMA (10 mL) was reacted with pyrrolidine (0.55 mL, 6.6 mmol) and heated to 60° C. for 3 hours. The mixture was then cooled and quenched with H2O and acidified with citric acid. The mixture was then extracted with ethyl acetate, dried with MgSO4, and concentrated. The residue was triturated with diethyl ether/hexanes and the solid filtered and dried (0.87 g). A portion of the solid (0.500 g, 1.28 mmol) was dissolved in DMF and reacted with ethyl iodide (1.0 mL, 12.77 mmol) and sodium hydride (0.060 g, 1.5 mmol). The mixture was stirred for 16 hours. The mixture was quenched with H2O and extracted with ethyl acetate. The organic layers were combined, dried with sodium sulfate, and concentrated. The residue was triturated with diethyl ether and filtered to yield 0.25 g of the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06331538B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-bbe7ccc635db47c6bea040d0e8ed53ce |
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| Source note | uspto-grants-2001_12 |
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