HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583395Generated: October 31, 2026
Potassium Iodide → 2-Isopropyl-11-oxo-11H-pyrido[2,1-b]quinazoline-8-carboxylic acid 4-pyridin-3-yl-butyl ester
https://huagongshe.com/reaction/1583395
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 12562128 | HCID 12562128 | — |
| Reactant | 4-(3-Pyridinyl)butyl chloride | HCID 13999760 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Isopropyl-11-oxo-11H-pyrido[2,1-b]quinazoline-8-carboxylic acid 4-pyridin-3-yl-butyl ester | HCID 13557513 | 44.6% |
Reaction Steps
A suspension of 0.70 g of 2-(1-methylethyl)-11-oxo-11H-pyrido[2,1-b]quinazoline-8-carboxylic acid, 0.50 g of 4-(3-pyridinyl)butylchloride, 0.40 g of potassium iodide and 0.39 g of potassium carbonate in 12 ml of dimethylformamide was stirred over night at a bath temperature of 50° C. The reaction mixture was diluted with ethylacetate, washed with water, dried (potassium carbonate) and concentrated. The residue was chromatographed on 75 g of silica gel eluting with ethyl acetate to give 0.46 g of a yellow solid which was recrystallized from ethyl acetate-hexane to give 0.33 g (32%), mp 95°-96° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04551460 |
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| Source dataset | uspto-grants-1985_11 |
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| ORD ID | ord-e442beb8ab094892863502f88436e092 |
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| Source note | uspto-grants-1985_11 |
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