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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 473594생성일: 2026년 10월 26일

Piperazin-2-one → 1-Boc-3-(3-oxo-1-piperazinyl)azetidine

https://huagongshe.com/reaction/473594

반응식

참여 물질

역할이름HCID투입량
반응물Piperazin-2-oneHCID 231360—
반응물3-Oxo-azetidine-1-carboxylic acid tert-butyl esterHCID 1519404—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매1,2-DichloroethaneHCID 11—
용매Acetic AcidHCID 176—
생성물1-Boc-3-(3-oxo-1-piperazinyl)azetidineHCID 5960543968.9%

반응 단계

To a mixture of 3-oxopiperazine 4a (490 mg, 4.89 mmol) and N-Boc-azetidin-3-one 1a (922 mg, 5.38 mmol) in 1,2-dichloroethane (10 mL) and HOAc (0.5 mL) was added Na(OAc)3BH (1141, 5.38 mmol). The reaction was stirred at room temperature overnight. Additional 1a (335 mg, 1.96 mmol) and Na(OAc)3BH (415 mg, 1.96 mmol) was added. The reaction was stirred for another 24 h before it was quenched with aq. NaHCO3. The resulting mixture was extracted with CH2Cl2. The organic solution was dried over Na2SO4 and concentrated. Purification by column chromatography (silica gel, 4% MeOH/CH2Cl2) gave intermediate 4b as white solid (860 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637498B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-6c6a32182fe444da9fcb8db27933f73c
출처 메모uspto-grants-2014_01