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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661421Generated: October 30, 2026

Potassium Carbonate → HCID 11582016, compound

https://huagongshe.com/reaction/661421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,4-Diamino-6-chloropyrimidineHCID 67432—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 136041855HCID 136041855—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 11582016HCID 1158201612.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-{5-[(4-chlorophenyl)amino]-1,3,4-oxadiazol-2-yl}phenol (144.0 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 (100.0 mg, 0.5 mmol) was added and the reaction mixture was stirred with heating at 80° C. for 10 min, then 6-chloro-2,4-diamino-pyrimidine (72.3 mg, 0.5 mmol) was added, followed by anhydrous K2CO3 (34.5 mg, 0.25 mmol). Then the vial was capped and microwaved at 200° C. for 15 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. 40 mL of EtOAc and ca. 40 mL of saturated 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 beige solid (24.5 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084618B2
Source datasetuspto-grants-2011_12
ORD IDord-4ab1d0c70cbc4f61b48ed219dc871ba6
Source noteuspto-grants-2011_12