반응식
[Cl:1][CH2:2][C:3](Cl)=[O:4].[NH2:6][C:7]1[C:12]([CH3:13])=[CH:11][C:10]([Br:14])=[CH:9][N:8]=1.C(N(CC)CC)C>C(Cl)Cl>[Br:14][C:10]1[CH:11]=[C:12]([CH3:13])[C:7]([NH:6][C:3](=[O:4])[CH2:2][Cl:1])=[N:8][CH:9]=1참가 물질
5
실험 절차
1.75 mL (22 mmol) chloroacetyl chloride are added to a solution, cooled to 0° C., of 3.74 g (20 mmol) 2-amino-5-bromo-3-methylpyridine in 50 mL DCM and then 6.1 mL (44 mmol) triethylamine are slowly added dropwise. After the addition has ended the ice bath is removed and the reaction mixture is stirred for 4 h at RT. It is poured onto water, extracted exhaustively with DCM, the combined organic phases are washed with water and saturated NaCl solution and dried over Na2SO4. After the desiccant and solvent have been eliminated the residue is purified by chromatography (silica gel, cyc/EtOAc 2:1).
후처리
- additionAfter the addition
- customis removed
- additionIt is poured onto water
- extractionextracted exhaustively with DCM
- washthe combined organic phases are washed with water and saturated NaCl solution
- dry with materialdried over Na2SO4
- customis purified by chromatography (silica gel, cyc/EtOAc 2:1)
출처 및 근거
- ORD 기록
- ord-4aede1005bfe4e03826578031574b8ca
- 출처 데이터셋
- uspto-grants-2013_12
- 특허 번호
- US08618132B2
연결된 노트
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