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HRID 572082作成日:2026年10月25日

Sodium Hydroxide → 2,2,2-Trichloroethyl 3-tert-butyl-1-(4-cyanophenyl)-1H-pyrazol-5-ylcarbamate

https://huagongshe.com/reaction/572082

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物2,2,2-Trichloroethyl chloroformateHCID 87063—
反応物4-(5-Amino-3-tert-butyl-1H-pyrazol-1-yl)benzonitrileHCID 7147083—
溶媒Ethyl AcetateHCID 8857—
生成物2,2,2-Trichloroethyl 3-tert-butyl-1-(4-cyanophenyl)-1H-pyrazol-5-ylcarbamateHCID 6878250979.1%

反応手順

To a suspension of Intermediate 14a (2.28 g, 9.49 mmol) in EtOAc (25 mL) and aq. NaOH solution (1M, 23.7 mL, 23.7 mmol) was added 2,2,2-trichloroethyl chloroformate (1.57 mL, 11.4 mmol) dropwise over 2 min. A precipitate formed which redissolved after 15 min, then the orange solution was stirred at RT for 90 min. 2,2,2-Trichloroethyl chloroformate (0.391 mL, 2.85 mmol) was added, and the orange mixture stirred at RT for 16 h. The layers were separated, and the aqueous extracted with EtOAc (25 mL). The combined organics were washed with brine (25 mL), dried (Na2SO4), filtered and concentrated in vacuo to leave an orange-red oil. Recrystallisation from cyclohexane gave an off-white solid (3.12 g, 79%). LCMS (Method 3): Rt 4.46 min, m/z 415, 417 [MH+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09029373B2
出典データセットuspto-grants-2015_05
ORD IDord-df31bdc81579404eaf8c23f782223f95
出典メモuspto-grants-2015_05