반응식
[NH:1]([C:11]([O:13][CH2:14][CH:15]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[C:21]2[C:16]1=[CH:17][CH:18]=[CH:19][CH:20]=2)=[O:12])[C@H:2]([C:8]([OH:10])=[O:9])[CH2:3][CH2:4][CH2:5][CH2:6][NH2:7].Cl.[CH3:29][N:30]1[CH:34]=[CH:33][N:32]=[C:31]1[CH:35]=O.[BH-](O[C:47]([CH3:49])=O)(OC(C)=O)OC(C)=O.[Na+].O>ClCCCl>[CH:17]1[C:16]2[CH:15]([CH2:14][O:13][C:11]([NH:1][C@@H:2]([CH2:3][CH2:4][CH2:5][CH2:6][N:7]([CH2:35][C:31]3[N:30]([CH3:29])[CH:47]=[CH:49][N:32]=3)[CH2:35][C:31]3[N:30]([CH3:29])[CH:34]=[CH:33][N:32]=3)[C:8]([OH:10])=[O:9])=[O:12])[C:27]3[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=3)[C:21]=2[CH:20]=[CH:19][CH:18]=1참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 0 °C
실험 절차
A solution of Fmoc-Lys-OH.HCl (1.822 g, 4.5 mmol) and 1-methyl-1H-imidazole-2-carbaldehyde (1.10 g, 10 mmol) in DCE (50 mL) was stirred at 75° C. for 30 min under nitrogen. The reaction mixture was cooled to 0° C., and treated with NaBH(OAc)3 (3.165 g, 15 mmol). The reaction mixture was stirred at room temperature for overnight and decomposed with water. The reaction mixture was extracted with DCM, the organic layer dried and concentrated under reduced pressure. The residue was purified by flash chromatography over silica gel to afford (S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-6-(bis((1-methyl-1H-imidazol-2-yl)methyl)amino)hexanoic acid (2.30 g, 92%). MS (ESI), 557 (M+H)+.
후처리
- extractionThe reaction mixture was extracted with DCM
- customthe organic layer dried
- concentrationconcentrated under reduced pressure
- customThe residue was purified by flash chromatography over silica gel
출처 및 근거
- ORD 기록
- ord-3762fa1087c0450da700c054388e2c27
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08840865B2
연결된 노트
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