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HRID 473593作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物3-Oxo-azetidine-1-carboxylic acid tert-butyl esterHCID 1519404—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物3-Oxo-4-pyrimidin-2-yl-piperazine-1-carboxylic acid tert-butyl esterHCID 66823688—
溶媒1,2-DichloroethaneHCID 11—
溶媒Acetic AcidHCID 176—
溶媒DichloromethaneHCID 6344—
溶媒Trifluoroacetic acidHCID 6422—
生成物3-(3-Oxo-4-pyrimidin-2-yl-piperazin-1-yl)-azetidine-1-carboxylic acid tert-butyl esterHCID 6683624910.5%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08637498B2
出典データセットuspto-grants-2014_01
ORD IDord-e2272eb4ff46483387dd6f0643ba0185
出典メモuspto-grants-2014_01