Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394373Generated: November 3, 2026

2-Thiophenecarbonyl chloride → HCID 18973068, compound

https://huagongshe.com/reaction/2394373

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenecarbonyl chlorideHCID 78928—
ReactantHCID 18973025HCID 18973025—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductHCID 18973068HCID 18973068—

Reaction Steps

To a solution of 5-chloro-1-ethyl-7-azaoxindole (400 mg, 2.03 mmol) and 4-dimethylaminopyridine (537 mg, 4.4 mmol) in DMF (10 mL) at 0° C. was added thiophene-2-carbonyl chloride (0.24 mL, 2.24 mmol). The reaction mixture was stirred at room temperature for 2 hours and then poured into ice/water. The mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, dried (magnesium sulfate) and concentrated in vacuo. The residue was chromatographed on a column of silica gel eluting with chloroform. Fractions containing only the desired product were combined and concentrated to afford the title compound as a solid which was recrystallized from hexanes. The yield of recrystallized material was 29 mg (50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811432
Source datasetuspto-grants-1998_09
ORD IDord-b4fa863a1e2445b79ae0c25ac7dacf81
Source noteuspto-grants-1998_09