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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611159Generated: November 2, 2026

Acetic Acid → HCID 136050744, compound

https://huagongshe.com/reaction/1611159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 22258874HCID 22258874—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 136050744HCID 13605074476%

Reaction Steps

A suspension of tert-butyl 3-{2-amino-6-[2,6-bis(benzyloxy)phenyl]-3-cyano-4-pyridinyl}-1-piperidinecarboxylate (3.46 g, 5.9 mmol) and Pd/C (10%, 600 mg) in ethyl acetate (50 mL) including acetic acid (5 mL) was stirred for 2 days at room temperature under a hydrogen atmosphere. The reaction mixture was diluted with THF (200 mL) and filtered through Celite®. The filtrate was concentrated under reduced pressure. The residue was washed with ethyl acetate and hexane, and dried under reduced pressure to give tert-butyl 3-[2-amino-3-cyano-6-(2,6-dihydroxyphenyl)-4-pyridinyl]-1-piperidinecarboxylate (1.82 g, yield; 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06984649B1
Source datasetuspto-grants-2006_01
ORD IDord-a1b7c71c572e4330aa5b79f13f09e842
Source noteuspto-grants-2006_01