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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1668518생성일: 2026년 10월 26일

tert-Butyl piperazine-1-carboxylate → t-Butyl 4-(6-chloromethylpyridin-2-ylmethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1668518

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물2,6-Bis(chloromethyl)pyridineHCID 316654—
용매EthanolHCID 702—
생성물t-Butyl 4-(6-chloromethylpyridin-2-ylmethyl)piperazine-1-carboxylateHCID 5810522838.4%

반응 단계

2,6-Bis(chloromethyl)pyridine (352 mg) was suspended in 4 mL of ethanol, and 372 mg of N-(t-butoxycarbonyl)piperazine was added into the suspension at ice temperature, and then the suspension was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure, the residue was added to water and extracted with chloroform. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and the solvent was removed. The residue was purified by chromatography on silica gel (methylene chloride-ethanol=30:1) to give 250 mg of t-butyl 4-(6-chloromethylpyridin-2-ylmethyl)piperazine-1-carboxylate as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07989446B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-da6258bb609641c28feb59f6b6ced1c4
출처 메모uspto-grants-2011_08