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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1835302생성일: 2026년 10월 26일

Sodium Hydroxide → 4-{5-[(3,5-Bis-trifluoromethyl-benzyl)-methyl-carbamoyl]-4-o-tolyl-pyridin-2-yl}-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1835302

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물3,5-Bis(trifluoromethyl)benzyl bromideHCID 122573—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
반응물4-(5-Methylcarbamoyl-4-o-tolyl-pyridin-2-yl)-piperazine-1-carboxylic acid tert-butyl esterHCID 54387824—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물4-{5-[(3,5-Bis-trifluoromethyl-benzyl)-methyl-carbamoyl]-4-o-tolyl-pyridin-2-yl}-piperazine-1-carboxylic acid tert-butyl esterHCID 985231970.8%

반응 단계

To a solution of 6.28 g (15.3 mmol) 4-(5-methylcarbamoyl-4-o-tolyl-pyridin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester in 250 ml tetrahydrofuran 20 ml of a 1 M solution (20 mmol) of potassium hexamethyldisilazide in tetrahydrofuran were added at 0° C. After 30 min, 2.81 ml (15.3 mmol) 3,5-bis(trifluoromethyl)benzyl bromide were added dropwise. The reaction mixture was allowed to warm to room temperature over night. Addition of water and 1 M aqueous sodium hydroxide solution was followed by extraction with three portions of ethyl acetate. The combined organic extracts were dried with sodium sulfate and concentrated. Flash column chromatography gave 6.89 g (70.8%) of the title compound as a white solid. MS m/e (%): 637 (M+H+, 100).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06770637B2
출처 데이터셋uspto-grants-2004_08
ORD IDord-d0c0aa4545d5477ca90f4ee9133e1507
출처 메모uspto-grants-2004_08