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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105216Generated: October 31, 2026

4-(N-Boc-amino)piperidine → HCID 68816915, compound

https://huagongshe.com/reaction/2105216

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(N-Boc-amino)piperidineHCID 723833—
ReactantHCID 11281654HCID 11281654—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 68816915HCID 6881691565.3%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 6-chloro-2-{2-[3-(pyrid-2-yl)isoxazol-5-yl]pyrrolidin-1-yl}-4-(5-methyl-1H-pyrazol-3-ylamino)pyrimidine (Example 17) (150 mg, 0.35 mmol) and 4-(N-tert-butoxycarbonylamino)piperidine (700 mg, 3.5 mmol) were added to dioxane (4 ml) and heated in a sealed vessel under microwave irradiation at 150° C. for 60 minutes. The crude reaction mixture was purified by reverse phase HPLC using a C18 column eluting with water/acetonitrile/TFA (95:5:0.2 decreasing in polarity to 0:100:0.2). The product containing fractions were passed down an SCX-2 column eluting with methanol and then releasing the product with 2N methanolic ammonia. The solvent was removed by evaporation to give the title compound (134 mg, 64%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579349B2
Source datasetuspto-grants-2009_08
ORD IDord-1cdfa196a26541d09cd49928b858bdf3
Source noteuspto-grants-2009_08