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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1949150Generated: October 25, 2026

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

https://huagongshe.com/reaction/1949150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantTriethylamineHCID 8471—
Reactant(2-Thienylmethyl)amineHCID 34005—
Reactant2-Chloroquinoline-3-carboxylic acidHCID 847163—
SolventThionyl ChlorideHCID 24386—
Product2-chloro-N-(thiophen-2-ylmethyl)quinoline-3-carboxamideHCID 8664533848%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399673B2
Source datasetuspto-grants-2013_03
ORD IDord-86a2f937289f468ba8a929400e90d358
Source noteuspto-grants-2013_03