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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433503Generated: October 26, 2026

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

https://huagongshe.com/reaction/1433503

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 numberUS07612092B2
Source datasetuspto-grants-2009_11
ORD IDord-f9141b74442440e68235fbd6a4f2907c
Source noteuspto-grants-2009_11