Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tetrahydrofuran → 1-(5-Bromopyrimidin-2-yl)ethan-1-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | 5-Bromopyrimidine-2-carbonitrile | HCID 686546 | — |
| 반응물 | HCID 178418573 | HCID 178418573 | — |
| 생성물 | 1-(5-Bromopyrimidin-2-yl)ethan-1-one | HCID 53488064 | 26% |
반응 단계
To a stirred solution of 5-bromo-2-cyanopyrimidine (600 mg, 3.26 mmol) in THF (40 mL) at −78° C. was added methylmagnesium bromide (1.4M solution, 7 mL, 9.78 mmol). The reaction mixture was stirred for an additional 20 minutes until LC/MS analysis indicated that the reaction was complete. Quenching with saturated NH4Cl, extraction with EtOAc and drying over MgSO4, afforded the crude residue which was purified by flash column chromatography, gradient elution (0 to 50%) hexane/ethyl acetate, to afford compound Int-2a as a white solid (170 mg, 26% yield). HPLC-MS tR=0.54 min (UV254 nm); mass calculated for formula C6H5BrN2O 199.96, observed LCMS m/z 201.0 (M+H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09227971B2 |
| 출처 데이터셋 | uspto-grants-2016_01 |
| ORD ID | ord-f16827ef7c29400dbd59ab2c26225c7d |
| 출처 메모 | uspto-grants-2016_01 |