반응식
[C:1]([N:8]1[CH2:13][CH2:12]O[CH2:10][CH:9]1[C:14]([OH:16])=[O:15])([O:3]C(C)(C)C)=O.[CH3:17]N(C(O[N:25]1N=N[C:27]2C=CC=C[C:26]1=2)=[N+](C)C)C.[B-](F)(F)(F)F.[CH:39]([N:42]([CH:45]([CH3:47])[CH3:46])[CH2:43][CH3:44])([CH3:41])[CH3:40].[Cl:48]CCl>>[ClH:48].[CH3:17][O:16][C:14](=[O:15])[C@@H:9]([CH3:10])[NH2:8].[CH:39]([N:42]([CH:45]([CH3:47])[CH3:46])[CH2:43][CH3:44])([CH3:41])[CH3:40].[CH3:27][C@@H:26]1[C:1](=[O:3])[N:8]2[CH2:13][CH2:12][NH:42][CH2:10][CH:9]2[C:14](=[O:16])[NH:25]1참가 물질
반응물 4
생성물 3
실험 절차
To a solution of N-boc-morpholine-3-carboxylic acid (2 g, 9.379 mmol) in 60 mL of dichloromethane and was added TBTU (3.313 g, 10.32 mmol) and diisopropylethyl amine (1.96 mL, 11.25 mmol). The reaction was stirred for 30 min. In the meantime, a solution of D-alanine methyl ester hydrochloride (1.93 g, 18.76 mmol) and diisopropylethylamine (3.27 mL, 18.76 mmol) in 20 mL of dichloromethane was prepared and finally added to the reaction mixture. The reaction was left stirring at room temperature for 2 h. UPLC-MS analysis showed the expected product (peak at 0.60 min, m/z=317 (M+1), 261 (M−t-Bu+1), 217 (M−Boc+1)). The reaction was diluted with dichloromethane and extracted with sat. NaHCO3, dried (Na2SO4), and the solvent removed. The crude (5.56 g) was taken to the next step without further purification.
후처리
- additionfinally added to the reaction mixture
- waitThe reaction was left
- stirringstirring at room temperature for 2 h
- extractionextracted with sat. NaHCO3
- dry with materialdried (Na2SO4)
- customthe solvent removed
- customThe crude (5.56 g) was taken to the next step without further purification
출처 및 근거
- ORD 기록
- ord-fca0426383df493bb055573c88de7bea
- 출처 데이터셋
- uspto-grants-2012_01
- 특허 번호
- US08097618B2
연결된 노트
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