Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Piperazin-2-one → 1-Boc-3-(3-oxo-1-piperazinyl)azetidine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Piperazin-2-one | HCID 231360 | — |
| 반응물 | 3-Oxo-azetidine-1-carboxylic acid tert-butyl ester | HCID 1519404 | — |
| 반응물 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | 1-Boc-3-(3-oxo-1-piperazinyl)azetidine | HCID 59605439 | 68.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08637498B2 |
| 출처 데이터셋 | uspto-grants-2014_01 |
| ORD ID | ord-6c6a32182fe444da9fcb8db27933f73c |
| 출처 메모 | uspto-grants-2014_01 |