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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantBinap, (A+-)-HCID 634876—
Reactantrel-(2R,6S)-2,6-dimethylpiperazineHCID 6950261—
Reactant1-Acetyl-6-bromo-5-methoxyindolineHCID 21948375—
Catalystpalladium(II) acetateHCID 167845—
Productcis-1-Acetyl-6-(3,5-dimethylpiperazin-1-yl)-5-methoxyindolineHCID 6966490663.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109201B2
Source datasetuspto-grants-2006_09
ORD IDord-c0694c3c82f34c59bff5cd6f16af9d04
Source noteuspto-grants-2006_09