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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 636831생성일: 2026년 10월 26일

Dimethylformamide → 2-Benzyl-piperazine-1,2,4-tricarboxylic acid 1-benzyl ester 4-tert-butyl ester 2-methyl ester

https://huagongshe.com/reaction/636831

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Benzyl BromideHCID 7498—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
반응물1-Benzyl 4-tert-butyl 2-methyl piperazine-1,2,4-tricarboxylateHCID 4451965—
용매TetrahydrofuranHCID 8028—
생성물2-Benzyl-piperazine-1,2,4-tricarboxylic acid 1-benzyl ester 4-tert-butyl ester 2-methyl esterHCID 53692857—

반응 조건

온도-78 °C

반응 단계

To a stirred solution of piperazine-1,2,4-tricarboxylic acid 1-benzyl ester 4-tert-butyl ester 2-methyl ester (20.0 g, 53 mmol) in tetrahydrofuran (500 mL) under nitrogen was added N,N-dimethylformamide (50 mL). The reaction was cooled to about −78° C., and a 1 M solution of sodium bis(trimethylsilyl)amide in tetrahydrofuran (80 mL) was added. The reaction was stirred at about −78° C. for about 1 hour, and then benzyl bromide (9.4 mL, 79 mmol) was added. The reaction was stirred for about 30 minutes more at about −78° C., then warmed to room temperature and stirred overnight. The reaction was quenched with saturated sodium bicarbonate solution, and the mixture was extracted three times with ethyl acetate. The combined organic layers were extracted twice with water, brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to give 31 g of crude product. Purification by silica gel chromatography using 10-20% ethyl acetate/hexanes as eluent afforded the title compound of part 4-A (20.3 g, 82%): +APcI MS (M−tBu+H)+ 413, (M−Boc+H)+ 369; 1H NMR=400 MHz (CDCl3) δ: 7.37 (arom, m, 5H), 7.22 (arom, m, 3H), 7.00 (arom, m, 2H), 1.41 (BOC, d, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06194578B1
출처 데이터셋uspto-grants-2001_02
ORD IDord-d3c9e9ed2ef04e6f927f567860022033
출처 메모uspto-grants-2001_02