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HRID 508613作成日:2026年10月24日

Pinacolone → 5-tert-Butyl-1-(4-methanesulfonyl-phenyl)-1H-pyrazole-3-carboxylic acid ethyl ester

https://huagongshe.com/ja/reaction/508613

反応式

関与物質

役割名称HCID仕込み量
反応物PinacoloneHCID 6416—
反応物Diethyl OxalateHCID 7268—
反応物4-(Methylsulphonyl)phenylhydrazineHCID 70142—
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
溶媒EthanolHCID 702—
溶媒TetrahydrofuranHCID 8028—
生成物5-tert-Butyl-1-(4-methanesulfonyl-phenyl)-1H-pyrazole-3-carboxylic acid ethyl esterHCID 5964934657%

反応手順

To a solution of 1M NaHMDS in THF in 120 mL of THF was added dropwise pinacolin (3.1 mL, 25 mmol) at 78° C. After 1 hour, diethyl oxalate (3.7 mL, 27.5 mmol) was added dropwise. The reaction mixture was allowed to warm up to room temperature and stirred overnight. The reaction was quenched by adding 1N HCl solution (50 mL). The reaction mixture was extracted with EtOAc and dried with MgSO4. The mixture was concentrated in vacuo. The product 2h was used without further purification. To a solution of 2h (1 g, 5 mmol) in EtOH (50 mL) was added 4-methylsulfonylphenylhydrazine 1a (1.22 g, 5.5 mmol) at room temperature. The reaction mixture was stirred overnight and refluxed for 3 hour. After cooling, the solvent was removed in vacuo. The resulting solid was purified by column chromatography with hexanes/EtOAc (1:1) to afford the titled compound (1 g, 57% yield) as a white solid. mp 174.9-177.6° C. 1H NMR (300 MHz, DMSO-d6): δ 8.11 (d, J=9 Hz, 2H), 7.80 (d, J=9 Hz, 2H), 6.76 (s, 1H), 4.27 (q, J=7 Hz, 2H), 3.35 (s, 3H), 1.27 (t, J=7 Hz, 3H), 1.16 (s, 9H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09096532B2
出典データセットuspto-grants-2015_08
ORD IDord-f6a56d8d4be1467b83ca038eeb0a6c16
出典メモuspto-grants-2015_08