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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Bromo-1-[tert-butyl(dimethyl)silyl]-1H-indole | HCID 11472373 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | tert-Butyl 3-benzylpiperazine-1-carboxylate | HCID 44118664 | — |
| Catalyst | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59381924 | HCID 59381924 | 74.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07754721B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-826123f264c64f698585ee43f7cf6ce2 |
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| Source note | uspto-grants-2010_07 |
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