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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843014Generated: October 30, 2026

HCID 18727259, compound → HCID 18727271, compound

https://huagongshe.com/reaction/843014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18727259HCID 18727259—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuran ethanolHCID 21873804—
ProductHCID 18727271HCID 1872727183%

Reaction Steps

A suspension of 10% Pd/C (0.20 g) and N-benzyloxy-N-methyl-1-[4-(5-fluoroindol-3-yl)piperidine-1-sulfonyl]piperidine-2-(R)-carboxamide (0.40 g, 0.75 mmol) [prepared as described in Step 4 above] in 80% ethanol/tetrahydrofuran (6 ml) was stirred under a hydrogen atmosphere (1 atm) for 70 min. The reaction was degassed with nitrogen, filtered through is Celite and the filtrate was concentrated in vacuo. The residue was chromatographed (PTLC, SiO2, 10% methanol/methylene chloride) to give N-hydroxy-N-methyl-1-[4-(5-fluoroindol-3-yl)piperidine-1-sulfonyl]piperidine-2-(R)-carboxamide (83%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376506B1
Source datasetuspto-grants-2002_04
ORD IDord-09b16af3ec0d4ed8a17a029499a1972c
Source noteuspto-grants-2002_04