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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730582Generated: October 29, 2026

HCID 57834996, compound → HCID 57834973, compound

https://huagongshe.com/reaction/730582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57834996HCID 57834996—
SolventEthanolHCID 702—
SolventHydrazineHCID 9321—
ProductHCID 57834973HCID 5783497316.1%

Reaction Steps

4-[1-(3-Fluoro-benzyl)-2,3-dioxo-2,3-dihydro-1H-indol-4-yl]-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester (930 mg) was dissolved in 17 ml each of hydrazine and ethanol, and the solution was heated at 110° C. for 16 hours. The reaction was cooled and partitioned between water and ethyl acetate, and the organic phase was dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by chromatography to afford 146 mg of 4-[1-(3-fluoro-benzyl)-2-oxo-2,3-dihydro-1H-indol-4-yl]-piperidine-1-carboxylic acid tert-butyl ester. MS: 423 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582760B2
Source datasetuspto-grants-2009_09
ORD IDord-d056d7b75b564026a84b61c93181848e
Source noteuspto-grants-2009_09