Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994047Generated: October 27, 2026

Potassium Carbonate → 6-(4-{5-[(3-Chlorophenyl)amino]-1,3,4-oxadiazol-2-yl}phenoxy) pyrimidine-2,4-diamine

https://huagongshe.com/reaction/1994047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,4-Diamino-6-chloropyrimidineHCID 67432—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant4-[5-(3-Chloro-phenylamino)-[1,3,4]oxadiazol-2-yl]-phenolHCID 136179696—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
Product6-(4-{5-[(3-Chlorophenyl)amino]-1,3,4-oxadiazol-2-yl}phenoxy) pyrimidine-2,4-diamineHCID 1161093731.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-{5-[(3-chlorophenyl)amino]-1,3,4-oxadiazol-2-yl}phenol (143.8 mg, 0.5 mmol) was dissolved in 3 mL of anhydrous DMF in a 2-5 mL microwave vial (Personal Chemistry). Solid potassium bis(trimethylsilyl)amide (200.0 mg, 1.0 mmol) was added and the reaction mixture was stirred with heating at 80° C. for 10 min, then 6-chloro-2,4-diamino-pyrimidine (86.7 mg, 0.6 mmol) was added, followed by anhydrous K2CO3 (69.1 mg, 0.5 mmol). Then the vial was capped and microwaved at 180° C. for 40 min. Then the reaction mixture was diluted with ca. 1 mL of MeOH, filtered through 0.22 um syringe filter and purified by reverse-phase preparative HPLC in acetonitrile/water system with 0.01% TFA. Fractions, containing the product, were partitioned between ca. 50 mL of EtOAc and ca. 50 mL of saturated aqueous NaHCO3. EtOAc layer was washed with brine, dried over anhydrous Na2SO4 and filtered. Solvent was removed in vacuo to give the title product as a light-yellow solid (62.0 mg). Yield 31.3%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652051B2
Source datasetuspto-grants-2010_01
ORD IDord-900663e711834eac9b7d6a6ce7ae1b4e
Source noteuspto-grants-2010_01