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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672154Generated: October 26, 2026

Water → 1-benzyl-3-(tetrahydro-pyran-4-ylmethyl)-4-(1-triisopropylsilanyl-1H-indazol-5-yl)-piperazin-2-one

https://huagongshe.com/reaction/1672154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-(Bromomethyl)oxaneHCID 2773286—
Reactant1-benzyl-4-(1-triisopropylsilanyl-1H-indazol-5-yl)-piperazin-2-oneHCID 67335395—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
Product1-benzyl-3-(tetrahydro-pyran-4-ylmethyl)-4-(1-triisopropylsilanyl-1H-indazol-5-yl)-piperazin-2-oneHCID 6733671190%

Reaction Steps

To a solution of 1-benzyl-4-(1-triisopropylsilanyl-1H-indazol-5-yl)-piperazin-2-one (0.78 g, 1.7 mmol) in 8.5 mL THF at −78° C. was added sec-butyllitium (1.3 mL, 1.9 mmol) drop-wise over 5 minutes. After 30 minutes 4-bromomethyl-tetrahydropyran (0.36 g, 2.0 mmol) was added in one portion and mixture was warmed to room temperature. After 18 hours H2O was added and the mixture was extracted with ethyl acetate. The combined organic layerss were washed with H2O, brine, dried over NaSO4, filtered and concentrated in vacuo. Purification via flash chromatography afforded 1-benzyl-3-(tetrahydro-pyran-4-ylmethyl)-4-(1-triisopropylsilanyl-1H-indazol-5-yl)-piperazin-2-one (0.55g, 90%) as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998963B2
Source datasetuspto-grants-2011_08
ORD IDord-a34d32927d4145dcb8fb7e93531423d7
Source noteuspto-grants-2011_08