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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226861Generated: October 27, 2026

3-Chloro-5-methoxybenzo[b]thiophene-2-carboxamide → 5-Methoxy-3-[[2-(4-morpholinyl)ethyl]thio]benzo[b]thiophene-2-carboxamide

https://huagongshe.com/reaction/2226861

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-5-methoxybenzo[b]thiophene-2-carboxamideHCID 10681595—
Reactant4-Morpholineethanethiol hydrochlorideHCID 12336622—
Reactant3-(Cycloundecen-1-yl)-1,2-diazacycloundec-2-eneHCID 53630274—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-Methoxy-3-[[2-(4-morpholinyl)ethyl]thio]benzo[b]thiophene-2-carboxamideHCID 979860983%

Reaction Steps

Diazabicycloundecene (DBU) (990 μL, 6.62 mmol) is added to a suspension of 3-chloro-5-methoxybenzo[b]thiophene-2-carboxamide (200 mg, 0.83 mmol) and 4-morpholineethanethiol hydrochloride (608 mg, 3.31 mmol) in 4 mL of DMF. The mixture is stirred at room temperature for 3 hours then diluted with ethyl acetate and washed with water followed by aqueous citric acid. NaHCO3 is added to the acidic extracts and the precipitated solids are collected and washed with water. Recrystallization from methanol:water provides 5-methoxy-3-[[2-(4-morpholinyl)ethyl]thio]benzo[b]thiophene-2-carboxamide in 83% yield; mp=158.5°-159.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05350748
Source datasetuspto-grants-1994_09
ORD IDord-0b53ad9354fd439c83954c267e1e6b75
Source noteuspto-grants-1994_09