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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412273Generated: October 29, 2026

HCID 22258740, compound → HCID 22258804, compound

https://huagongshe.com/reaction/412273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22258740HCID 22258740—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
ProductHCID 22258804HCID 2225880473%

Reaction Steps

To a solution of tert-butyl 3-[2-amino-6-[2-(benzyloxy)phenyl]-3-(hydroxymethyl)-4-pyridinyl]-1-piperidinecarboxylate (0.900 g, 1.838 mmol) in methylene chloride (20 mL) was added manganese (IV) oxide (3.20 g, 36.8 mmol). After stirred at room temperature for 40 min, the mixture was filtered to remove the manganese salt. The filtrate was concentrated under reduced pressure. The resulting solid was purified by recrystallization from a mixture of ethyl acetate and hexane to give tert-butyl 3-[2-amino-6-[2-(benzyloxy)phenyl]-3-formyl-4-pyridinyl]-1-piperidinecarboxylate. (0.651 g, yield; 73%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562811B1
Source datasetuspto-grants-2003_05
ORD IDord-8fb877b2d35a4c239b8cbe49699557b0
Source noteuspto-grants-2003_05