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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994041Generated: October 30, 2026

Potassium Carbonate → HCID 11582016, compound

https://huagongshe.com/reaction/1994041

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 numberUS07652051B2
Source datasetuspto-grants-2010_01
ORD IDord-1aa3c5c7ff1e4ba688e97fa78fddc5a1
Source noteuspto-grants-2010_01