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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351331Generated: November 2, 2026

Triethylamine → [(Z)-[3-[[2-(4-fluorophenyl)-2-hydroxyethyl]-methylsulfamoyl]-5,6-dihydro-4H-1-benzothiophen-7-ylidene]amino] N-trimethylsilylcarbamate

https://huagongshe.com/reaction/1351331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantTrimethylsilyl isocyanateHCID 70696—
Reactant(7e)-7-Hydroxyimino-4,5,6,7-tetrahydro-benzo[b]thiophene-3-sulfonic acid[2-(4-fluorophenyl)-2-hydroxyethyl]-methyl-amideHCID 11350049—
SolventTolueneHCID 1140—
Product[(Z)-[3-[[2-(4-fluorophenyl)-2-hydroxyethyl]-methylsulfamoyl]-5,6-dihydro-4H-1-benzothiophen-7-ylidene]amino] N-trimethylsilylcarbamateHCID 140032406—

Reaction Steps

To a solution of the compound (1.0 g) of Example 1 in toluene (10 mL) was added triethylamine (1.75 mL) and trimethylsilyl isocyanate. After stirring at room temperature for 2 hours, the solution was dilutied with ethyl acetate, and the resulting insoluble matter was extracted, the crude product that were obtained by removing the solvent by evaporation was purified by NH-silica gel column chromatography (ethyl acetate/hexane), and a pale yellow oily substance (1.0 g) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217723B2
Source datasetuspto-grants-2007_05
ORD IDord-b713f7560c904fadb51aeb23c24d0818
Source noteuspto-grants-2007_05