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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875778Generated: October 29, 2026

(3R)-3-Aminopiperidine, 3-BOC protected → HCID 67045184, compound

https://huagongshe.com/reaction/875778

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3R)-3-Aminopiperidine, 3-BOC protectedHCID 1514172—
ReactantHCID 60205468HCID 60205468—
Solvent1-ButanolHCID 263—
ProductHCID 67045184HCID 6704518431.2%

Reaction Conditions

Temperature155 °C

Reaction Steps

A mixture of N-(5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)-3-chloro-4-fluorobenzamide (240 mg, 0.621 mmol) and (R)-tert-butyl piperidin-3-ylcarbamate (373 mg, 1.86 mmol) in n-BuOH (3 mL) was stirred at 155° C. for 16 hours in a sealed tube. The reaction was then cooled to room temperature and concentrated in vacuo. The resulting residue was purified by reverse phase HPLC (Gilson) to provide (R)-tert-butyl 1-(5-bromo-3-(3-chloro-4-fluorobenzamido)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperidin-3-ylcarbamate (110 mg, 31% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981085B2
Source datasetuspto-grants-2015_03
ORD IDord-88d2fddc04de4b72822ae9d6412278cf
Source noteuspto-grants-2015_03