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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897838Generated: November 2, 2026

Trifluoroacetic acid → HCID 58399754, compound

https://huagongshe.com/reaction/1897838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 67237662HCID 67237662—
SolventEthyl AcetateHCID 8857—
ProductHCID 58399754HCID 58399754—

Reaction Steps

Trifluoroacetic acid in an amount of 40 equivalents was added to the obtained tert-butyl 4-[9-methyl-6-(2,3-dihydro-2-oxo-1-tert-butoxycarbonyl-1H-thieno[3,4-d]imidazol-4-yl)-9H-carbazol-3-yl]-2,3-dihydro-2-oxo-1H-thieno[3,4-d]imidazole-1-carboxylate and a reaction was carried out at 25° C. for 3 hours. The resulting reaction liquid was dropped slowly to a saturated aqueous sodium carbonate solution to neutralize, thereby stopping the reaction. Ethyl acetate was added to the reaction liquid and stirred, and then an organic layer was taken and the solvent was distilled off. The residue was purified by silica gel column chromatography using an ethyl acetate/hexane solvent, so that 4-[9-methyl-6-(2,3-dihydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl)-9H-carbazol-3-yl]-2,3-dihydro-1H-thieno[3,4-d]imidazol-2-one was obtained. The yield based on the charged tert-butyl 4-[9-methyl-6-(2,3-dihydro-2-oxo-1-tert-butoxycarbonyl-1H-thieno[3,4-d]imidazol-4-yl)-9H-carbazol 3-yl]-2,3-dihydro-2-oxo-1H-thieno[3,4-d]imidazole-1-carboxy late was 90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519150B2
Source datasetuspto-grants-2013_08
ORD IDord-6b2d46dc6b5243f5bc2c103aaa54d024
Source noteuspto-grants-2013_08