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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373429Generated: October 30, 2026

Water → HCID 56946484, compound

https://huagongshe.com/reaction/2373429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantHCID 56946380HCID 56946380—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 56946484HCID 56946484—

Reaction Conditions

Temperature1 °C

Reaction Steps

To a solution of 2-(3,4-dimethoxy-phenylamino)-9-iodo-5H,7H-benzo[b]pyrimido[4,5-d]azepin-6-one (I-30) (100 mg, 0.210 mmol) in 4 mL anhydrous DMF at room temperature was added zinc cyanide (14 mg, 0.120 mmol), tris(dibenzylideneacetone)dipalladium (9.5 mg, 0.01 mmol), 1,1′-bis(diphenyl-phosphino)ferrocene (14.0 mg, 0.02 mmol) and a drop of H2O. The solution was degassed with argon then stirred at 1° C. for 16 h. The solution was allowed to cool to 22° C., then diluted with EtOAc and saturated aqueous sodium bicarbonate. The organic layer was then washed with H2O and brine, dried over Na2SO4, and concentrated in vacuo. The product was recrystallized in methanol and CH2Cl2 to give I-92 (92%): MS Rt═2.49 min, m/z═388 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459448B2
Source datasetuspto-grants-2008_12
ORD IDord-da1fbb0e418246bfa09aaef98628ae68
Source noteuspto-grants-2008_12