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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034788Generated: November 1, 2026

(3R)-3-Aminopiperidine, 3-BOC protected → HCID 67045135, compound

https://huagongshe.com/reaction/1034788

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3R)-3-Aminopiperidine, 3-BOC protectedHCID 1514172—
ReactantHCID 60205480HCID 60205480—
Solvent1-ButanolHCID 263—
ProductHCID 67045135HCID 6704513569%

Reaction Steps

A mixture of N-(5-bromo-4-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)-3-(trifluoromethyl)benzamide (250 mg, 0.622 mmol) and (R)-tert-butyl piperidin-3-ylcarbamate (374 mg, 1.87 mmol) in n-BuOH (3 mL) was processed as described in Example 62, Step B, to provide (R)-tert-butyl 1-(5-bromo-3-(3-(trifluoromethyl)benzamido)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperidin-3-ylcarbamate (250 mg, 69% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08545897B2
Source datasetuspto-grants-2013_10
ORD IDord-769c5e4f3a8646998b4ba181d18185c4
Source noteuspto-grants-2013_10