Methylamine → HCID 17838151, 화합물
반응식
CN.[NH:3]1[C:11]2[C:6](=[CH:7][C:8]([NH:12][CH:13]3[CH2:18][CH2:17][CH2:16][N:15]([CH:19]([C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=4)[C:20](O)=[O:21])[CH2:14]3)=[CH:9][CH:10]=2)[CH:5]=[N:4]1.Cl.[CH2:30]([N:32]=C=NCCCN(C)C)C.ON1C2C=CC=CC=2N=N1.CN(C1C=CC=CN=1)C.C(=O)([O-])O.[Na+]>CN(C)C=O>[CH3:30][NH:32][C:20](=[O:21])[CH:19]([N:15]1[CH2:16][CH2:17][CH2:18][CH:13]([NH:12][C:8]2[CH:7]=[C:6]3[C:11](=[CH:10][CH:9]=2)[NH:3][N:4]=[CH:5]3)[CH2:14]1)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1참가 물질
반응물 6
생성물 1
시약·촉매·용매 1
실험 절차
Methylamine (30 mg) and the compound prepared in Example 222 (88 mg) were dissolved in dimethylformamide (1 ml), and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (86 mg), 1-hydroxybenzotriazole (77 mg), and dimethylaminopyridine (5 mg) were added to the solution. The reaction mixture was stirred at room temperature for 18 hr. A saturated aqueous sodium hydrogencarbonate solution (1 ml) was then added thereto, and the mixture was extracted with chloroform-propanol (3/1). The organic layer was dried over anhydrous sodium sulfate, and the solvent was removed by distillation under the reduced pressure. The residue was purified by HPLC [chloroform/methanol] to give 52 mg of the title compound as two diastereomers (ratio=ca. 50:50).
후처리
- extractionthe mixture was extracted with chloroform-propanol (3/1)
- dry with materialThe organic layer was dried over anhydrous sodium sulfate
- customthe solvent was removed by distillation under the reduced pressure
- customThe residue was purified by HPLC [chloroform/methanol]
출처 및 근거
- ORD 기록
- ord-89b2f044a552440e8b5d9f4f30c79384
- 출처 데이터셋
- uspto-grants-2007_05
- 특허 번호
- US07217722B2
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