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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 473593생성일: 2026년 10월 26일

3-Oxo-azetidine-1-carboxylic acid tert-butyl ester → 3-(3-Oxo-4-pyrimidin-2-yl-piperazin-1-yl)-azetidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/473593

반응식

참여 물질

역할이름HCID투입량
반응물3-Oxo-azetidine-1-carboxylic acid tert-butyl esterHCID 1519404—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물3-Oxo-4-pyrimidin-2-yl-piperazine-1-carboxylic acid tert-butyl esterHCID 66823688—
용매1,2-DichloroethaneHCID 11—
용매Acetic AcidHCID 176—
용매DichloromethaneHCID 6344—
용매Trifluoroacetic acidHCID 6422—
생성물3-(3-Oxo-4-pyrimidin-2-yl-piperazin-1-yl)-azetidine-1-carboxylic acid tert-butyl esterHCID 6683624910.5%

반응 단계

A solution of intermediate 3b (120 mg, 0.43 mmol) in TFA (0.75 mL) and CH2Cl2 (3 mL) was stirred at room temperature for 1.5 h. The solution was concentrated. The resulting residue was stirred with N-Boc-azetidin-3-one 1a (81 mg, 0.47 mmol) and Na(OAc)3BH (100, 0.47 mmol) in 1,2-dichloroethane (4 mL) and HOAc (0.2 mL) at room temperature overnight. The reaction 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, 3% MeOH/CH2Cl2) gave intermediate 3c as light yellow solid (15 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637498B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-e2272eb4ff46483387dd6f0643ba0185
출처 메모uspto-grants-2014_01