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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 609696Generated: October 29, 2026

HCID 18727259, compound → HCID 18727271, compound

https://huagongshe.com/reaction/609696

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]piperdine-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 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 numberUS05998412
Source datasetuspto-grants-1999_12
ORD IDord-5d2f809ce1b141fbbfd582413b2cfb85
Source noteuspto-grants-1999_12