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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674715Generated: October 26, 2026

Dimethylformamide → 4-[9-Methyl-6-oxo-2-(2,3,4-trifluorophenoxy)-6,9-dihydro-1H-purin-1-yl]benzonitrile

https://huagongshe.com/reaction/1674715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1-(4-Bromophenyl)-9-methyl-2-(2,3,4-trifluorophenoxy)-1,9-dihydro-6H-purin-6-oneHCID 24744032—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
Product4-[9-Methyl-6-oxo-2-(2,3,4-trifluorophenoxy)-6,9-dihydro-1H-purin-1-yl]benzonitrileHCID 57614145—

Reaction Conditions

Temperature120 °C

Reaction Steps

1-(4-Bromophenyl)-9-methyl-2-(2,3,4-trifluorophenoxy)-1,9-dihydro-6H-purin-6-one (68 mg, 0.1507 mmol), Zn(CN)2 (10.6 mg, 0.0904 mmol), Pd2(dba)3 (4.1 mg, 0.0045 mmol) and 1,1′-bis(diphenylphosphino)ferrocene (5.0 mg, 0.0090 mmol) are added to DMF (1.2 mL) and H2O (0.012 mL). The mixture is purged with N2 for 3 min and then heated at 120° C. for 18 h. The mixture is passed through celite. Water (30 mL) is added and the resulting mixture is extracted with CH2Cl2 (50 mL×4). After drying the CH2Cl2 over MgSO4, the solvent is removed in vacuo. The crude product is purified by column chromatography (MeOH:CH2Cl2=2:98) to afford the title compound as a brown solid. 1H NMR (400 MHz, CDCl3) 7.86 (2H, d, J 8), 7.65 (1H, s), 7.53 (2 h, d, J 8), 6.95 (2H, m), 3.59 (3H, s). MS (M+1): 398.03; RT=1.22 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003656B2
Source datasetuspto-grants-2011_08
ORD IDord-8ea6785b39ab4e8594fda3ef475be87d
Source noteuspto-grants-2011_08