반응식
Br[C:2]1[C:10]2[C:9]([Cl:11])=[N:8][CH:7]=[N:6][C:5]=2[NH:4][CH:3]=1.[Li]CCCC.CN([CH:20]=[O:21])C>C1COCC1>[Cl:11][C:9]1[C:10]2[C:2]([CH:20]=[O:21])=[CH:3][NH:4][C:5]=2[N:6]=[CH:7][N:8]=1참가 물질
반응 조건
- 온도
- -78 °C
실험 절차
To a solution of 5-bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine (2.33 g, 10.0 mmol, 1.0 eq) in anhydrous THF (100 mL) at −78° C. under argon, n-BuLi solution (2.5 M in THF, 8.8 mL, 22.0 mmol, 2.2 eq) was added dropwise (over 10 min). The resulting mixture was stirred at −78° C. for 1 h and then DMF (2.0 g, 11.0 mmol, 1.1 eq) was added dropwise (over 10 min). The mixture was stirred at −78° C. for an additional 30 min and then stirred at RT overnight. The reaction mixture was quenched with H2O (50 mL) and then concentrated in vacuo. The residue was triturated with saturated aqueous NH4Cl solution. The solid was collected by filtration, rinsed with ethyl acetate, and dried in vacuo to afford 4-chloro-7H-pyrrolo[2,3-d]pyrimidine-5-carbaldehyde (1.17 g, 65% yield).
후처리
- stirringThe mixture was stirred at −78° C. for an additional 30 min
- stirringstirred at RT overnight
- customThe reaction mixture was quenched with H2O (50 mL)
- concentrationconcentrated in vacuo
- customThe residue was triturated with saturated aqueous NH4Cl solution
- filtrationThe solid was collected by filtration
- washrinsed with ethyl acetate
- customdried in vacuo
출처 및 근거
- ORD 기록
- ord-f48b0753ae664f3ab9d90fc2b28b9892
- 출처 데이터셋
- uspto-grants-2015_03
- 특허 번호
- US08969363B2
연결된 노트
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