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HRID 1994047作成日:2026年10月26日

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

https://huagongshe.com/reaction/1994047

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2,4-Diamino-6-chloropyrimidineHCID 67432—
反応物Potassium bis(trimethylsilyl)amideHCID 3251421—
反応物4-[5-(3-Chloro-phenylamino)-[1,3,4]oxadiazol-2-yl]-phenolHCID 136179696—
溶媒MethanolHCID 887—
溶媒DimethylformamideHCID 6228—
生成物6-(4-{5-[(3-Chlorophenyl)amino]-1,3,4-oxadiazol-2-yl}phenoxy) pyrimidine-2,4-diamineHCID 1161093731.3%

反応条件

温度80 °C

反応手順

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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07652051B2
出典データセットuspto-grants-2010_01
ORD IDord-900663e711834eac9b7d6a6ce7ae1b4e
出典メモuspto-grants-2010_01