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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533757Generated: October 30, 2026

(4-Aminophenoxy)benzene → HCID 46843517, compound

https://huagongshe.com/reaction/533757

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Aminophenoxy)benzeneHCID 8764—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
ReactantHCID 58064817HCID 58064817—
Catalystpalladium(II) acetateHCID 167845—
Solvent2-Methyl-2-butanolHCID 6405—
ProductHCID 46843517HCID 4684351726.7%

Reaction Conditions

Temperature95 °C

Reaction Steps

3-Chloro-5,7,8,9-tetrahydro-dipyrido[2,3-b;3′,4′-d]pyrrole-6-carboxylic acid tert-butyl ester (100 mg, 0.32 mmol), 4-phenoxyaniline (120 mg, 0.65 mmol), Pd(OAc)2 (3 mg, 0.01 mmol), X-Phos (12 mg, 0.03 mmol), and KOH (0.03 ml, 0.97 mmol) were suspended in tert-amyl alcohol (2 mL), and stirred overnight at 95° C. The crude mixture was added directly to a Biotage column. The crude product was purified via Biotage eluting with a gradient of 0 to 100% EtOAc in hexanes to provide 43 (39 mg, 26% yield) as a brown solid. LC-MS (M+H=457, obsd.=457).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853391B2
Source datasetuspto-grants-2014_10
ORD IDord-4cc73b02cc9b43379a6585abe732ca10
Source noteuspto-grants-2014_10