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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Benzyl Bromide | HCID 7498 | — |
| 반응물 | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| 반응물 | 1-Benzyl 4-tert-butyl 2-methyl piperazine-1,2,4-tricarboxylate | HCID 4451965 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-Benzyl-piperazine-1,2,4-tricarboxylic acid 1-benzyl ester 4-tert-butyl ester 2-methyl ester | HCID 53692857 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06194578B1 |
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| 출처 데이터셋 | uspto-grants-2001_02 |
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| ORD ID | ord-d3c9e9ed2ef04e6f927f567860022033 |
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| 출처 메모 | uspto-grants-2001_02 |
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