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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724962Generated: October 30, 2026

2,6-Di-tert-butyl-4-methylphenol → 13-Benzyl-2-ethyl-9-methyl-2,4,9,15-tetraazatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3,5,7,12,14-hexaen-10-one

https://huagongshe.com/reaction/724962

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Di-tert-butyl-4-methylphenolHCID 31404—
ReactantStannane, tributyl(phenylmethyl)-HCID 141419—
ReactantPotassium FluorideHCID 522689—
ReactantHCID 10547779HCID 10547779—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
Product13-Benzyl-2-ethyl-9-methyl-2,4,9,15-tetraazatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3,5,7,12,14-hexaen-10-oneHCID 470723—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 5,11-dihydro-11-ethyl-8-iodo-5-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one (0.3 g, 0.79 mmol), bis(triphenylphosphine)palladium(II) chloride (18 mg, 0.03 mmol), and 2,6-di-tert-butyl-4-methylphenol (1 crystal) in 5 mL of N,N-dimethylformamide was added benzyltributylstannane (0.36 g, 0.94 mmol). The resultant reaction mixture was heated at 100° C. under argon for 5 hours. An aqueous solution of potassium fluoride was added and the mixture was stirred for 5 hours. The product was extracted with dichloromethane and purified by flash chromatography, eluting with ethyl acetate/dichloromethane, to give 20 mg of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05705499
Source datasetuspto-grants-1998_01
ORD IDord-9179948f6de94dbb8baf60c010db5789
Source noteuspto-grants-1998_01