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HRID 473594作成日:2026年10月26日

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

https://huagongshe.com/reaction/473594

反応式

関与物質

役割名称HCID仕込み量
反応物Piperazin-2-oneHCID 231360—
反応物3-Oxo-azetidine-1-carboxylic acid tert-butyl esterHCID 1519404—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒1,2-DichloroethaneHCID 11—
溶媒Acetic AcidHCID 176—
生成物1-Boc-3-(3-oxo-1-piperazinyl)azetidineHCID 5960543968.9%

反応手順

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).

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-6c6a32182fe444da9fcb8db27933f73c
出典メモuspto-grants-2014_01