반응식
Br[C:2]1[C:10]2[C:5]([NH:6][CH:7]=[N:8][C:9]=2[Cl:11])=[N:4][CH:3]=1.C([Li])CCC.Cl[C:18]([O:20][CH2:21][CH3:22])=[O:19].[NH4+].[Cl-]>C1COCC1>[Cl:11][C:9]1[C:10]2[C:2]([C:18]([O:20][CH2:21][CH3:22])=[O:19])=[CH:3][NH:4][C:5]=2[N:6]=[CH:7][N:8]=1참가 물질
반응 조건
- 온도
- -78 °C
실험 절차
A solution of 5-bromo-4-chloropyrrolo[2,3-d]pyrimidine (Example 35) (232 mg; 1 mmol) in anhydrous THF (5 mL) was cooled to -78° C. under argon and a solution of n-butyl lithium (1.3 mL of 2.31M) was added at such a rate that the temperature of the reaction mixture remained below -72° C. After stirring the reaction mixture at -78° C. for 45 minutes, a solution of ethyl chloroformate (0.15 mL) in THF (2 ml) was added slowly, maintaining the reaction temperature below -72° C. The reaction mixture was stirred at -78° C. for 2 hours then allowed to warn to room temperature. A saturated solution of NH4Cl (20 mL) was added to the reaction mixture. The organic layer was separated and the aqueous layer was extracted with ethyl acetate (2×25 mL). The combined organic extracts were dried and evaporated to a white solid, yield 210 mg (92%): m.p. 140°-141° C.
후처리
- customremained below -72° C
- temperaturemaintaining the reaction temperature below -72° C
- stirringThe reaction mixture was stirred at -78° C. for 2 hours
- customto warn to room temperature
- customThe organic layer was separated
- extractionthe aqueous layer was extracted with ethyl acetate (2×25 mL)
- customThe combined organic extracts were dried
- customevaporated to a white solid, yield 210 mg (92%)
출처 및 근거
- ORD 기록
- ord-32aa1718c12b4011bb6032f0522da1c6
- 출처 데이터셋
- uspto-grants-1999_01
- 특허 번호
- US05864033
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