HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214752Generated: October 25, 2026
Cesium carbonate → cis-1-Acetyl-6-(3,5-dimethylpiperazin-1-yl)-5-methoxyindoline
https://huagongshe.com/reaction/2214752
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | rel-(2R,6S)-2,6-dimethylpiperazine | HCID 6950261 | — |
| Reactant | 1-Acetyl-6-bromo-5-methoxyindoline | HCID 21948375 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | cis-1-Acetyl-6-(3,5-dimethylpiperazin-1-yl)-5-methoxyindoline | HCID 69664906 | 63.2% |
Reaction Steps
A mixture of palladium (II) acetate (830 mg, 3.7 mmole), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (3.46 g, 5.5 mmole) and cesium carbonate (18.1 g, 56 mmole) in dry degassed 1,4-dioxane (200 ml) under argon was sonicated at 28° C. for 0.5 h producing a pink heterogeneous mixture. This was treated with D1 (10 g, 37 mmole) followed by cis-2,6-dimethylpiperazine (12.6 g, 110 mmole) and heated with rapid stirring at reflux for 96 h. The mixture was allowed to cool, filtered through Kieselguhr and then concentrated under vacuum. The residue was treated with EtOAc and 2M HCl acid, shaken well and the aqueous layer separated, basified by addition of K2CO3 and extracted with DCM. The extract was dried (Na2SO4) and concentrated under vacuum to afford the title compound as a pale orange solid (7.1 g, 63%). MH+ 304.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07109201B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-c0694c3c82f34c59bff5cd6f16af9d04 |
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| Source note | uspto-grants-2006_09 |
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