HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576052Generated: October 31, 2026
Trifluoroacetic acid → HCID 86707270, compound
https://huagongshe.com/reaction/576052
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86707271 | HCID 86707271 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Anisole | HCID 7519 | — |
| Product | HCID 86707270 | HCID 86707270 | — |
Reaction Steps
Trifluoroacetic acid (1 mL) was added to a solution of N-(2,4-dimethoxybenzyl)-N-{2-fluoro-4-[2-(pyridin-2-yl)ethoxy]phenyl}-2-(trifluoroacetyl)-1,2,3,4-tetrahydroisoquinoline-6-sulfonamide obtained (350 mg) in a mixture of anisole (5 mL) and chloroform (5 mL) while cooling in ice, and the mixture was stirred at room temperature for 16 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution while cooling in ice, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and 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 (hexane:ethyl acetate=70:30→chloroform:methanol=95:5) to afford N-{2-fluoro-4-[2-(pyridin-2-yl)ethoxy]phenyl}-2-(trifluoroacetyl)-1,2,3,4-tetrahydroisoquinoline-6-sulfonamide as a colorless oil (12 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-4c30079a3a7d469a9fef4169b4bcaa49 |
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| Source note | uspto-grants-2015_05 |
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