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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105143Generated: November 3, 2026

Bromoform → 4-bromo-2-[[(2,3-difluorophenyl)methyl]thio]-7(8H)-pteridinone

https://huagongshe.com/reaction/2105143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoformHCID 5558—
ReactantIsoamyl NitriteHCID 8053—
Reactant4-amino-2-[[(2,3-difluorophenyl)methyl]thio]-7(8H)-pteridinoneHCID 22320081—
SolventDimethyl SulfoxideHCID 679—
Product4-bromo-2-[[(2,3-difluorophenyl)methyl]thio]-7(8H)-pteridinoneHCID 22320082—

Reaction Conditions

Temperature125 °C

Reaction Steps

The product of step (a) (0.5 g) was suspended in DMSO (10 ml) and bromoform (10 ml) and the mixture was heated to 125° C. Isoamylnitrite (2 ml) was added and the mixture was stirred at 125° C. for 5 minutes before being cooled in an ice bath. Solvent was removed by evaporation under high vacuum and the residue suspended in dichloromethane (100 ml). This suspension was washed with saturated aqueous ammonium chloride (50 ml) and then filtered through a plug of celite. The filtrate was evaporated and purified by column chromatography, eluting with 10% ethyl acetate in dichloromethane to give the subtitled compound as a white solid (0.22 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579342B2
Source datasetuspto-grants-2009_08
ORD IDord-c578947adf6144f8af2c6b1852c52e7a
Source noteuspto-grants-2009_08