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HRID 450390作成日:2026年10月27日

Diisopropylethylamine → 2-Chloro-N-(5-methyl-1H-pyrazol-3-yl)-5-nitro-N-(tetrahydro-2H-pyran-4-yl)pyrimidine-4,6-diamine

https://huagongshe.com/reaction/450390

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物1H-Pyrazol-3-amine, 5-methyl-HCID 93146—
反応物2,4,6-Trichloro-5-nitropyrimidineHCID 4297843—
反応物2H-pyran-4-amineHCID 17791271—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物2-Chloro-N-(5-methyl-1H-pyrazol-3-yl)-5-nitro-N-(tetrahydro-2H-pyran-4-yl)pyrimidine-4,6-diamineHCID 86649284—

反応手順

To a solution of 2,4,6-trichloro-5-nitro pyrimidine (Intermediate 37, 1 g, 4.4 mmol) in EtOH at −50° C. were added 5-methyl-1H-pyrazol-3-amine (255 mg) and DIPEA (1.6 ml) drop-wise. The resulting mixture was stirred at this temperature for 5 minutes whereupon 4-amino pyran (300 mg) was added. The resulting mixture was allowed to warm to ambient temperature for 4 hours. The mixture was diluted with H2O and EtOAc and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with brine, saturated NaHCO3 (aq) solution, dried and evaporation of the volatiles under reduced pressure gave a colored residue. Purification by Gilson (MeCN/H2O, 5%→95%, 15 minutes) gave the title compound (120 mg). LCMS: 354 [M+1].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08486966B2
出典データセットuspto-grants-2013_07
ORD IDord-0cac8eba3950473ca5dbaaedd86949aa
出典メモuspto-grants-2013_07