HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730584Generated: October 29, 2026
HCID 57834979, compound → HCID 57834976, compound
https://huagongshe.com/reaction/730584
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57834979 | HCID 57834979 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57834976 | HCID 57834976 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582760B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-059e6786f1174bb3b3f406ece68fab70 |
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| Source note | uspto-grants-2009_09 |
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