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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 352225생성일: 2026년 10월 25일

1-Acetylpiperazine → (4-Acetyl-piperazin-1-yl)pyridin-3-yl-acetic acid ethyl ester

https://huagongshe.com/reaction/352225

반응식

참여 물질

역할이름HCID투입량
반응물1-AcetylpiperazineHCID 83795—
반응물Ethyl 2-bromo-2-(pyridin-3-yl)acetateHCID 21985933—
생성물(4-Acetyl-piperazin-1-yl)pyridin-3-yl-acetic acid ethyl esterHCID 6984940760%

반응 단계

N-acetyl-piperazine (3.7 g; 28.8 mmol; 2.8 equiv) was combined with bromo-pyridin-3-yl-acetic acid ethyl ester (approx. 2.5 g; 10 mmol). Purification on a 3×16 cm silica column using a 30% then 40% ethyl acetate/hexanes (v/v) mobile phase followed by a 2% methanol/dichloromethane (v/v) mobile phase resulted in 1.84 g light yellow oil (approx. 60% yield). MS(ES) calc'd: [M+H]+=292.2 m/z; [M+Na]+=314.2 m/z.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06743794B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-5f7765389b5b496bb3641e9d3af6995f
출처 메모uspto-grants-2004_06