HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922485Generated: October 30, 2026
Trifluoroacetic acid → HCID 117877605, compound
https://huagongshe.com/reaction/922485
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 117877607 | HCID 117877607 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 117877605 | HCID 117877605 | 92.4% |
Reaction Steps
To a solution of methyl [3-(5-{1-[(tert-butoxycarbonyl)(cyclopropyl)amino]ethyl}-2-ethylpyridin-3-yl)propyl]carbamate (204 mg) in dichloromethane (1.5 mL) was added trifluoroacetic acid (1.5 mL) under ice-cooling, and the mixture was stirred at room temperature for 1 hour. The reaction solution was poured into ice-cooled aqueous saturated sodium hydrogen carbonate solution, and extracted with chloroform. The organic layer was washed with saturated saline, dried over sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by NH-silica gel column chromatography (eluent: chloroform→chloroform/methanol=21/1) to give methyl (3-{5-[1-(cyclopropylamino)ethyl]-2-ethylpyridin-3-yl}propyl)carbamate [REx(113-8)] (142 mg) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278944B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-75ab3618882648ffaa30bb379205eba5 |
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| Source note | uspto-grants-2016_03 |
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