HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626812Generated: November 3, 2026
Trifluoroacetic acid → HCID 68196376, compound
https://huagongshe.com/reaction/1626812
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 68196375 | HCID 68196375 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68196376 | HCID 68196376 | 90% |
Reaction Steps
Ethyl({[5-(benzyloxy)-2-({1-[2-chloro-4′-(hydroxymethyl)biphenyl-4-yl]piperidin-4-yl}methyl)-6-methylpyrimidin-4-yl]carbonyl}amino)acetate (0.96 g, 1.5 mmol) was dissolved in dichloromethane (20 mL), and trifluoroacetic acid (20 mL) was added under a nitrogen atmosphere, followed by stirring at room temperature for 7 hours. An aqueous sodium hydrogencarbonate solution was added to the reaction solution for neutralization, followed by extraction with dichloromethane, and subsequently the organic layer was concentrated under reduced pressure. The resulting residue was purified by chromatography on a silica gel column (Moritex Corporation, elution solvent: dichloromethane/ethyl acetate), and a fraction corresponding to the Rf value=0.80 (dichloromethane/ethyl acetate=4/1) by thin layer chromatography was concentrated under reduced pressure to afford the title compound (0.74 g, 1.3 mmol) as a yellow oil (yield 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785462B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-f80510ef1ad3467b926a620c7334425e |
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| Source note | uspto-grants-2014_07 |
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