HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277969Generated: November 1, 2026
Propylene Oxide → Ethyl 5-bromoimidazo-[1,2-a]-quinoline-2-carboxylate
https://huagongshe.com/reaction/1277969
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propylene Oxide | HCID 6378 | — |
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | 4-Bromoquinolin-2-amine | HCID 14067419 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Ethyl 5-bromoimidazo-[1,2-a]-quinoline-2-carboxylate | HCID 12763980 | — |
Reaction Steps
1 g of 2-amino-4-bromoquinoline was dissolved in 20 ml of dimethoxyethane and a mixture of 1.5 g of ethyl bromopyruvate and 0.5 g of propylene oxide was added thereto. The solution was allowed to stand at room temperature for 1 hour and the quaternary salt thus precipitated was filtered off, was washed with ether and then was dissolved in 20 ml of ethanol. The solution was refluxed for 1 hour, cooled and then was evaporated to dryness under vacuum. The residue was partitioned between 50 ml of chloroform and 50 ml of 2 N sodium carbonate and the organic extract was washed with 50 ml of water, was dried over MgSO4, and was reduced in volume under vacuum. Then, ether was added thereto to give cream needles of ethyl 5-bromoimidazo-[1,2-a]-quinoline-2-carboxylate melting at 205°-207° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04279912 |
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| Source dataset | uspto-grants-1981_07 |
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| ORD ID | ord-d5aba955bfc34ba0b11ccd5bb94f10c6 |
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| Source note | uspto-grants-1981_07 |
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