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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(N-Boc-amino)piperidine | HCID 723833 | — |
| Reactant | HCID 11281654 | HCID 11281654 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 68816915 | HCID 68816915 | 65.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07579349B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-1cdfa196a26541d09cd49928b858bdf3 |
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| Source note | uspto-grants-2009_08 |
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