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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408303Generated: October 30, 2026

(3R)-3-Aminopiperidine, 3-BOC protected → HCID 67045343, compound

https://huagongshe.com/reaction/408303

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3R)-3-Aminopiperidine, 3-BOC protectedHCID 1514172—
ReactantHCID 60205484HCID 60205484—
Solvent1-ButanolHCID 263—
ProductHCID 67045343HCID 67045343—

Reaction Steps

A mixture of N-(5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-methylpyrazine-2-carboxamide (280 mg, 0.800 mmol) and (R)-tert-butyl piperidin-3-ylcarbamate (480 mg, 2.40 mmol) in n-BuOH (3 mL) was processed as described in Example 62, Step B, to provide crude (R)-tert-butyl 1-(5-bromo-3-(5-methylpyrazine-2-carboxamido)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperidin-3-ylcarbamate without HPLC purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08758830B2
Source datasetuspto-grants-2014_06
ORD IDord-13f6d68113e94818aaf056e7cee0de99
Source noteuspto-grants-2014_06