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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730584Generated: October 29, 2026

HCID 57834979, compound → HCID 57834976, compound

https://huagongshe.com/reaction/730584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57834979HCID 57834979—
ReactantHCID 178418348HCID 178418348—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57834976HCID 57834976—

Reaction Conditions

Temperature-78 °C

Reaction Steps

4-[1-(3-Fluoro-benzyl)-2,3-dioxo-2,3-dihydro-1H-indol-4-yl]-piperazine-1-carboxylic acid tert-butyl ester (330 mg) was dissolved in 4 mL of THF and cooled to −78° C. before adding 1.6 M methyl lithium in hexaness (800 uL). The solution was stirred and warmed to room temperature, then stirred for an hour at room temperature. The reaction was quenched by addition of water and extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography afforded 315 mg of 4-[1-(3-fluoro-benzyl)-3-hydroxy-3-methyl-2-oxo-2,3-dihydro-1H-indol-4-yl]-piperazine-1-carboxylic acid tert-butyl ester. MS: 356 (M−Boc+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582760B2
Source datasetuspto-grants-2009_09
ORD IDord-059e6786f1174bb3b3f406ece68fab70
Source noteuspto-grants-2009_09