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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244595Generated: October 30, 2026

Diisopropylethylamine → ethyl 6-bromo-4-[[(2S)-2-methoxypropyl]amino]quinoline-3-carboxylate

https://huagongshe.com/reaction/244595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 6-bromo-4-chloroquinoline-3-carboxylateHCID 2764138—
Reactant(S)-2-Methoxypropan-1-amine hydrochlorideHCID 71607326—
SolventEthanolHCID 702—
Productethyl 6-bromo-4-[[(2S)-2-methoxypropyl]amino]quinoline-3-carboxylateHCID 68108432—

Reaction Steps

Suspend ethyl-6-bromo-4-chloro-quinoline-3-carboxylate (389 g, 1.24 mol) and (2S)-2-methoxypropan-1-amine, hydrochloride (171 g, 1.36 mol, 1.1 eq.) in ethanol (5.84 L). Add diisopropylethylamine (474 mL) and heat the mixture at 50° C. overnight. After 16 hours, cool the reaction to room temperature and concentrate in vacuo. Add methyl tert-butyl ether (2 L) to the residue and stir for 20 min. Filter the precipitate and wash it with methyl tert-butyl ether (2×250 mL). Concentrate the filtrate in vacuo to afford the titled compound in almost quantitative yield. The compound will be used in the next step without further purification. MS (ESI) m/z (M+H)+ 367.0, 369.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658668B2
Source datasetuspto-grants-2014_02
ORD IDord-6d5fa84e05894992a374e5e996b82bd8
Source noteuspto-grants-2014_02