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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354567Generated: October 31, 2026

5-Bromo-1-[tert-butyl(dimethyl)silyl]-1H-indole → HCID 59381924, compound

https://huagongshe.com/reaction/2354567

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-1-[tert-butyl(dimethyl)silyl]-1H-indoleHCID 11472373—
ReactantSodium t-butoxideHCID 23676156—
Reactanttert-Butyl 3-benzylpiperazine-1-carboxylateHCID 44118664—
CatalystTris(1,1-dimethylethyl)phosphineHCID 83681—
Catalystpalladium(II) acetateHCID 167845—
SolventO-XyleneHCID 7237—
SolventEthyl AcetateHCID 8857—
ProductHCID 59381924HCID 5938192474.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of Pd(OAc)2 (0.054 g, 0.2 mmol), NaOtBu (0.64 g, 6.6 mmol) in xylene (7.0 mL) in a screw-capped tube was added tBu3P (0.049 g, 0.2 mmol). After 10 minutes a solution of 5-bromo-1-(tert-butyl-dimethyl-silanyl)-1H-indole (1.30 g, 4.4 mmol) in xylene (7.0 mL) and a solution of 3-benzyl-piperazine-1-carboxylic acid tert-butyl ester (1.34 g, 4.8 mmol) in xylene (8.0 mL) were added. The mixture was heated to 80° C. for 30 minutes, then cooled to room temperature. The reaction mixture was taken up in ethyl acetate, filtered through a pad of celite, and concentrated under reduced pressure. Purification via flash chromatography (gradient: 2% to 20% EtOAc in hexane) afforded 3-Benzyl-4-[1-(tert-butyl-dimethyl-silanyl)-1H-indol-5-yl]-piperazine-1-carboxylic acid tert-butyl ester (1.65 g, 74%) as a pale yellow solid; MS (M+H)=506.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754721B2
Source datasetuspto-grants-2010_07
ORD IDord-826123f264c64f698585ee43f7cf6ce2
Source noteuspto-grants-2010_07