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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863102Generated: October 30, 2026

Triethylamine → 6-Methoxy-8-(1-methyl-4-phthalimidobutylamino)-4-(3-trifluoromethylstyryl)quinoline

https://huagongshe.com/reaction/1863102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-(4-Bromopentyl)phthalimideHCID 240534—
Reactant8-Amino-6-methoxy-4-(3-trifluoromethylstyryl)quinolineHCID 631320—
SolventChloroformHCID 6212—
Product6-Methoxy-8-(1-methyl-4-phthalimidobutylamino)-4-(3-trifluoromethylstyryl)quinolineHCID 63290178.6%

Reaction Steps

A mixture of 8.4 g (0.025 mole) of 8-amino-6-methoxy-4-(3-trifluoromethylstyryl)quinoline, 7.3 g (0.025 mole) of 4-bromo-1-phthalimidopentane and 2.5 g of triethylamine was heated in an oil bath at 130°-135° for 12 hr. The reaction mixture ws dissolved in chloroform and passed through a silica gel column to give 11 g of crude product which was used without further purification. Crystallization from ethanol provided an analytical sample as yellow needles, mp 154°-156°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04167638
Source datasetuspto-grants-1979_09
ORD IDord-e390b6d44cb54ab3b2826f1612d776c9
Source noteuspto-grants-1979_09