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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767361Generated: November 1, 2026

HCID 22258740, compound → HCID 22258804, compound

https://huagongshe.com/reaction/1767361

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-(hydroxy-methyl)-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-piperidine-carboxylate. (0.651 g, yield; 73%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07232909B2
Source datasetuspto-grants-2007_06
ORD IDord-de89dcea70a74dbf896dfcc4d1cb7423
Source noteuspto-grants-2007_06