Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753413Generated: October 27, 2026

2,4-Dichloro-5-fluoropyrimidine → N2,N4-bis(4-hydroxy-3-cyanophenyl)-5-fluoro-2,4-pyrimidinediamine

https://huagongshe.com/reaction/1753413

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-5-fluoropyrimidineHCID 250705—
Reactant5-Amino-2-hydroxybenzonitrileHCID 817719—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductN2,N4-bis(4-hydroxy-3-cyanophenyl)-5-fluoro-2,4-pyrimidinediamineHCID 22060861—

Reaction Conditions

Temperature70 °C

Reaction Steps

2,4-Dichloro-5-fluoropyrimidine (50 mg, 0.30 mmol) was dissolved in a mixture of MeOH (1 ml) and H2O (0.1 ml). 3-cyano-4-hydroxyaniline (241 mg, 1.8 mmol) was added and the mixture was refluxed for 2 days (70° C. oil-bath temperature). The mixture was cooled to 22° C., concentrated to dryness under reduced pressure and subjected to column chromatography on silica gel (CHCl3-Acetone, 9:1) to give N2,N4-bis(4-hydroxy-3-cyanophenyl)-5-fluoro-2,4-pyrimidinediamine. 1H NMR (CDCl3): δ 7.96 (d, 1H, J=3.5 Hz), 7.82 (d, 1H, J=3.0 Hz), 7.79 (d, 1H, J=3.0 Hz), 7.71 (dd, 1H, J=3.0, 8.8 Hz), 7.54 (dd, J=3.0, 8.8 Hz), 6.94 (d, 1H, J=8.8 Hz), 6.84 (d, 1H, J=8.8 Hz); LCMS: purity: 97.2%; MS (m/e): 362.98 (M+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09162989B2
Source datasetuspto-grants-2015_10
ORD IDord-281851f52ac0417d92d0b2a2a42cc5aa
Source noteuspto-grants-2015_10