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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577764Generated: October 30, 2026

Ethyl Acetate → (5-{[(3,5-Bis-trifluoromethyl-benzyl)-(5-methyl-isoxazol-3-yl)-amino]-methyl}-1,3-dimethyl-1h-pyrazolo[3,4-b]pyridin-6-yl)-cyclobutylmethyl-ethyl-amine

https://huagongshe.com/reaction/577764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant3,5-Bis(trifluoromethyl)benzyl bromideHCID 122573—
Reactantcyclobutylmethyl-{1,3-dimethyl-5-[(5-methyl-isoxazol-3-ylamino)-methyl]-1H-pyrazolo[3,4-b]pyridin-6-yl}-ethyl-amineHCID 58689766—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product(5-{[(3,5-Bis-trifluoromethyl-benzyl)-(5-methyl-isoxazol-3-yl)-amino]-methyl}-1,3-dimethyl-1h-pyrazolo[3,4-b]pyridin-6-yl)-cyclobutylmethyl-ethyl-amineHCID 1169283929%

Reaction Steps

Sodium hydride [0.06 g, (60% dispersion in mineral oil)] was added to a solution of cyclobutylmethyl-{1,3-dimethyl-5-[(5-methyl-isoxazol-3-ylamino)-methyl]-1H-pyrazolo[3,4-b]pyridin-6-yl}-ethyl-amine (0.225 g, 0.6 mmol) in anhydrous DMF (3 mL) while stirring at RT. After this mixture was stirred for 1 h, 3,5-bis-trifluoromethybenzyl bromide (0.13 mL, 0.7 mmol) was added slowly and stirring was continued for an additional 12 h. Ethyl acetate (30 mL) and water (30 mL) were added, and the layers were separated. The aqueous layer was back-extracted with ethyl acetate (2×30 mL). The combined organic extracts were washed with brine, dried over sodium sulfate, and concentrated in vacuo. The crude residue was purified by chromatography using silica gel (200-400 mesh) and eluted with 25-50% hexane:ethyl acetate to yield the title compound as a colorless thick liquid (0.10 g), yield: 29%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040558B2
Source datasetuspto-grants-2015_05
ORD IDord-65559e41806c4e7bbbfc816cb0cfe06f
Source noteuspto-grants-2015_05