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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719240Generated: October 31, 2026

Dichloromethane → HCID 21898040, compound

https://huagongshe.com/reaction/719240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
Reactant2,4-Dichloro-3-nitroquinolineHCID 2785138—
ReactantHCID 21898026HCID 21898026—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductHCID 21898040HCID 2189804033.9%

Reaction Conditions

Temperature21 °C

Reaction Steps

A solution of 2,4-dichloro-3-nitroquinoline (2.71 g, 0.0115 mole) in toluene (100 mL) was cooled to 0–5° C. in an ice bath. Triethylamine (1.5 g) was added in one portion. A solution of N-(10-amino-4,7-dioxadecyl)-5-dimethylaminonaphthalene-1-sulfonamide (4.6 g, 0.01159 mole) in toluene (60 mL) was added dropwise while maintaining the temperature below 10° C. The reaction was stirred at 2–5° C. for 4 hrs and at a room temperature of 21° C. overnight (18 hours). Thin layer chromatography (dichloromethane:ethanol) showed a trace of the amine starting material, but was mostly a bright yellow spot at the solvent front assumed to be the addition product. The toluene was removed by rotary evaporation to provide a viscous oil. The oil was purified by column chromatography (silica gel, dichloromethane/ethanol) to provide 2.4 g of N-[10-(2-chloro-3-nitro-4-quinolinyl)amino-4,7-dioxadecyl]-5-dimethylaminonaphthalene-1-sulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132429B2
Source datasetuspto-grants-2006_11
ORD IDord-9a560ad827ab43b2ba267757ab0f41e6
Source noteuspto-grants-2006_11