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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756504Generated: November 1, 2026

Allyl bromide → HCID 19390564, compound

https://huagongshe.com/reaction/1756504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Aminoquinoline-2-carboxylic acidHCID 22503957—
SolventDimethylformamideHCID 6228—
ProductHCID 19390564HCID 19390564—

Reaction Steps

4-Amino-2-quinoline carboxylic acid (800 mg, 4.2 mmol) in DMF (10 ml) and K2CO3 (1.17 g, 8.5 mmol) was stirred at ambient temperature in the presence of allyl bromide (1.47 ml, 17 mmol) for 24 hours. The solvent was evaporated and the crude residue purified by subjecting to silico-gel chromatography, eluting with petroleum ether ethyl acetate 1/1) to give 2-allyloxycarbonyl-4-amino-quinoline (170 mg, NMR (CDCls): δ4.75-5 (m, 4H); 5.2-5.0 (m, 2H); 5.9-6.35 (m, 1H); 7.35-8.3 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05441949
Source datasetuspto-grants-1995_08
ORD IDord-4cffe37e8603424c81bf6b93264f10b7
Source noteuspto-grants-1995_08