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HRID 2186220作成日:2026年10月25日

Methanol → 2-[Bis(tert-butoxycarbonyl)amino)-5-(2'-methylsulfonylphenyl)pyrimidine

https://huagongshe.com/reaction/2186220

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物2-[Bis(tert-butoxycarbonyl)amino]-5-(2'-methylthiophenyl)pyrimidineHCID 18177320—
反応物Potassium hydroxy sulfiteHCID 23707502—
溶媒WaterHCID 962—
生成物2-[Bis(tert-butoxycarbonyl)amino)-5-(2'-methylsulfonylphenyl)pyrimidineHCID 1817729356%

反応条件

温度0 °C

反応手順

2-[Bis(tert-butoxycarbonyl)amino]-5-(2′-methylthiophenyl)pyrimidine (2.13 g, 5.1 mmol) was dissolved in MeOH (20 mL) and cooled to 0° C. In a separate beaker, a solution of Oxone (5.49 g) was generated by dilution to 27 mL with water. A portion of this solution (17 mL, 5.6 mmol) was removed and adjusted to pH 4.2 with sat. Na3PO4 solution (4.7 mL). This mixture was added to the reaction and stirred 23 hours at room temp. The resulting mixture was diluted with water and extracted with CHCl3. The organics were combined, washed with water and brine, dried over Na2SO4, filtered, and evaporated. The crude product was chromatographed on silica gel (50-100% EtOAc/hexanes) to yield the sulfone (1.28 g, 56%). 1H NMR (CDCl3): δ8.81 (s, 2H), 8.28 (dd, 1H, J=7.6, J′=1.4), 7.72 (m, 2H), 7.39 (dd, 1H, J=7.3, J′=1.4), 2.76 (s, 3H), 1.50 (s, 18H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06403620B1
出典データセットuspto-grants-2002_06
ORD IDord-3c43d7f6bcb8442197a849ed75c8734e
出典メモuspto-grants-2002_06