Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853373Generated: October 26, 2026

Sodium Sulfide → 7-Methoxy-4-(5-nitrothiophen-2-ylsulfanyl)quinoline-6-carboxamide

https://huagongshe.com/reaction/853373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfideHCID 14804—
Reactant2-Bromo-5-nitrothiopheneHCID 83222—
Reactant4-Chloro-7-methoxyquinoline-6-carboxamideHCID 22936418—
SolventDimethylformamideHCID 6228—
Product7-Methoxy-4-(5-nitrothiophen-2-ylsulfanyl)quinoline-6-carboxamideHCID 2293662439%

Reaction Steps

4-Chloro-7-methoxyquinoline-6-carboxamide (1.18 g, 5.00 mmol)-and sodium sulfide (1.20 g, 5.50 mmol) were heated and stirred in dimethylformamide (10 ml) at 60° C. for 3 hours. After cooling the reaction solution to room temperature, 2-bromo-5-nitrothiophene (1.25 g, 6.00 mmol) was added and the mixture was further heated and stirred at 60° C. for 1 hour. The reaction solution was returned to room temperature and then poured into ice water (50 ml), and the precipitated crystals were filtered out, washed with water and methanol and then blow-dried to obtain the title compound (700 mg, 1.94 mmol, 39%) as yellowish-brown crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253286B2
Source datasetuspto-grants-2007_08
ORD IDord-040ba30eac7a4932aa292f502b6dd0e1
Source noteuspto-grants-2007_08