Bromide ion → HCID 178435592, 화합물
반응식
[Br-].[CH2:2]([Li])CCC.[PH4+].[CH2:8]([C:12]1[NH:13][C:14]2[C:19]([C:20](=[O:22])[N:21]=1)=[CH:18][C:17]([CH:23]=O)=[CH:16][CH:15]=2)[CH2:9][CH2:10][CH3:11]>O1CCCC1>[CH2:8]([C:12]1[NH:13][C:14]2[C:19]([C:20](=[O:22])[N:21]=1)=[CH:18][C:17]([CH:23]=[CH2:2])=[CH:16][CH:15]=2)[CH2:9][CH2:10][CH3:11]참가 물질
반응 조건
- 온도
- -78 °C
실험 절차
To a suspension of 15.14 g of mothyltriphenylphosphonium bromide in tetrahydrofuran, cooled to -78° C., is slowly added 21.73 ml of 1.95 M n-butyllithium in hexanes. The reaction mixture is allowed to warm to room temperature and stirred until all of the phosphonium salt dissolves. This takes approximately 30 minutes. The reaction mixture is cooled to -78° C. and 1.95 g of 2-butyl-1,4-dihydro-4-oxo-6-quinazolinecarboxaldehyde added in one portion as a solid. The reaction mixture is allowed to warm to room temperature and stirred for 18 hours. The reaction mixture is quenched with saturated ammonium chloride, diluted with water and extracted with ethyl acetate. The organic layer is separated, washed with briner dried with MgSO4 and concentrated in vacuo to a residue which is purified by chromatography on silica gel using 1:3 ethyl acetate-hexanes to give 2.48 g of the desired product as a solid. CI MASS SPEC 229 (M+H)
후처리
- temperatureto warm to room temperature
- dissolutiondissolves
- customThis takes approximately 30 minutes
- temperatureThe reaction mixture is cooled to -78° C.
- temperatureto warm to room temperature
- customThe reaction mixture is quenched with saturated ammonium chloride
- additiondiluted with water
- extractionextracted with ethyl acetate
- customThe organic layer is separated
- washwashed with briner
- dry with materialdried with MgSO4
- concentrationconcentrated in vacuo to a residue which
- customis purified by chromatography on silica gel using 1:3 ethyl acetate-hexanes
출처 및 근거
- ORD 기록
- ord-52b9c5e89abc46a0adec21ba147f37ea
- 출처 데이터셋
- uspto-grants-1994_03
- 특허 번호
- US05292734
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