HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576089Generated: October 29, 2026
Trifluoroacetic acid → HCID 86707297, compound
https://huagongshe.com/reaction/576089
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86707298 | HCID 86707298 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Anisole | HCID 7519 | — |
| Product | HCID 86707297 | HCID 86707297 | — |
Reaction Steps
Trifluoroacetic acid (0.2 mL) was added to a solution of 2-[1-(4-tert-butylphenyl)-2-methylpropan-2-yl]-N-(2,4-dimethoxybenzyl)-N-(4-fluorophenyl)-1,2,3,4-tetrahydroisoquinoline-6-sulfonamide obtained (22 mg) in a mixture of anisole (1 mL) and chloroform (1 mL) while cooling in ice, and the mixture was stirred for 2.5 hr while cooling in ice. Saturated aqueous sodium hydrogen carbonate solution was added to the reaction mixture while cooling in ice and the mixture was extracted with chloroform. The organic layer was dried over anhydrous magnesium sulfate and then the desiccant was filtered off, followed by concentration under reduced pressure. The resulting residue was purified by NH silica gel column chromatography (chloroform:methanol=49:1) to afford the title compound as a colorless oil (8 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09035059B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-162037be96cd424798619d7281aef2ea |
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| Source note | uspto-grants-2015_05 |
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