HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204012Generated: October 29, 2026
(3R)-3-Aminopiperidine, 3-BOC protected → HCID 67045415, compound
https://huagongshe.com/reaction/2204012
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (3R)-3-Aminopiperidine, 3-BOC protected | HCID 1514172 | — |
| Reactant | HCID 60205720 | HCID 60205720 | — |
| Solvent | (+-)-2-Butanol | HCID 6568 | — |
| Product | HCID 67045415 | HCID 67045415 | 46.7% |
Reaction Steps
(R)-tert-Butyl piperidin-3-ylcarbamate (307 mg, 1.53 mmol) was added to N-(4-fluoro-5-(2-methoxyethoxy)-1H-pyrrolo[2,3-b]pyridin-3-yl)cyclopropanecarboxamide (150 mg, 0.511 mmol) in s-BuOH (3 mL), and the reaction was stirred at 150° C. for 24 hours in a sealed tube. After cooling down and concentration, the residue was purified by reverse phase chromatography (SP4, 25M, water/ACN 90/10→0/100, 30 CV) to yield (R)-tert-butyl 1-(3-(cyclopropanecarboxamido)-5-(2-methoxyethoxy)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperidin-3-ylcarbamate (113 mg, 46.7% yield) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365568B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-89999171f8e34bebbd8f181ce6bf478c |
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| Source note | uspto-grants-2016_06 |
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