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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1949150Erstellt: 26. Oktober 2026

Hexane → 2-chloro-N-(thiophen-2-ylmethyl)quinoline-3-carboxamide

https://huagongshe.com/reaction/1949150

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexaneHCID 8058—
EduktTriethylamineHCID 8471—
Edukt(2-Thienylmethyl)amineHCID 34005—
Edukt2-Chloroquinoline-3-carboxylic acidHCID 847163—
LösungsmittelThionyl ChlorideHCID 24386—
Produkt2-chloro-N-(thiophen-2-ylmethyl)quinoline-3-carboxamideHCID 8664533848%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of 2.1 g (10.0 mmol) 2-chloroquinoline-3-carboxylic acid in thionyl chloride (60 ml) was heated for 2 h at 85° C. Then excess thionyl chloride was removed under vacuum. The residue was taken up with DCM (60 ml) and the solution was cooled to 0° C. and then mixed with 4.0 ml (30.0 mmol) NEt3 and 1.03 ml (10.0 mmol) thiophene-2-methylamine. After stirring for 90 min at RT it was diluted with EE and washed with a saturated aqueous NH4Cl solution. The aqueous phase was extracted with EE. The combined organic phases were washed with brine, dried over Na2SO4, filtered and concentrated to small volume under vacuum. Column chromatography (hexane/EE 4:1) with the residue yielded 1.44 g (4.8 mmol, 48%) 2-chloro-N-(thiophen-2-ylmethyl)quinoline-3-carboxamide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08399673B2
Quelldatensatzuspto-grants-2013_03
ORD IDord-86a2f937289f468ba8a929400e90d358
Quellennotizuspto-grants-2013_03