HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773402Generated: October 30, 2026
Trifluoroacetic acid → HCID 68671843, compound
https://huagongshe.com/reaction/1773402
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | N-Methyl-2-piperidone | HCID 13603 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 2-Amino-4-(4-methylpiperazin-1-yl) benzoic acid tertbutyl ester | HCID 66735920 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 68671843 | HCID 68671843 | 51% |
Reaction Steps
tert-Butyl 2-amino-4-(4-methylpiperazin-1-yl)benzoate (1.5 g, 5.15 mmol) was dissolved in dry dioxane (25 mL) under a nitrogen atmosphere. N-methylpiperidone (0.72 g, 6.18 mmol, 1.2 eq) was added, followed by trifluoroacetic acid (1.03 mL, 13.39 mmol, 2.6 eq) and sodium triacetoxyborohydride (1.72 g, 7.73 mmol, 1.5 eq). The mixture was stirred at room temperature for 26 hours. During this time extra portions of N-methylpiperidone (0.5 mL, 0.75 eq) and sodium triacetoxyborohydride (1.72 g, 7.73 mmol, 1.5 eq) were added. A saturated aqueous solution of NaHCO3 was then added and the reaction mixture was concentrated under reduced pressure. 10% ammonium hydroxide was added until pH 10 and the aqueous phase was extracted with dichloromethane. The organic phase was washed with brine, dried over Na2SO4 and evaporated under reduced pressure. After purification by chromatography over silica gel (DCM/MeOH/NH3 7% in MeOH 90:8:2) 1.025 g of title compound were obtained as off-white solid (51% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09255087B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-fad91913269c445eab57965ebd9e5dde |
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| Source note | uspto-grants-2016_02 |
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