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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814238Generated: November 2, 2026

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

https://huagongshe.com/reaction/1814238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoformHCID 5558—
ReactantAcetonitrileHCID 6342—
ReactantIsoamyl NitriteHCID 8053—
Reactant4-amino-2-[[(2,3-difluorophenyl)methyl]thio]-7(8H)-pteridinoneHCID 22320081—
SolventDimethyl SulfoxideHCID 679—
SolventDiethyl EtherHCID 3283—
Product4-bromo-2-[[(2,3-difluorophenyl)methyl]thio]-7(8H)-pteridinoneHCID 22320082—

Reaction Conditions

Temperature100 °C

Reaction Steps

The product of step (d) (6.0 g) was suspended in DMSO (90 ml) and bromoform (60 ml) was added and the mixture was heated to 100° C. Isopentylnitrite (25 ml) was added and the mixture stirred for 5 min. The mixture was quickly cooled in an ice bath then evaporated to leave an oil. This was repeated three times. Acetonitrile (200 ml) was added and the solid which separated was removed by filtration. The solvent was evaporated and the residue was purified by flash chromatography, eluting with dichloromethane and then 5% ethyl acetate in dichloromethane to give a yellow solid which was slurried with ether then collected. The solid was washed with ether and dried to give the subtitled compound as a colourless solid (8.74 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875868B2
Source datasetuspto-grants-2005_04
ORD IDord-e4193ce86b66477ca2d545426fdb5a3e
Source noteuspto-grants-2005_04