반응식
[F:1][C:2]1[CH:3]=[N:4][C:5]2[CH:6]=[CH:7][C:8](=[O:30])[N:9]3[CH2:13][C:12]([CH2:15][N:16]4[CH2:21][CH2:20][CH:19]([NH:22][C:23](=[O:29])[O:24][C:25]([CH3:28])([CH3:27])[CH3:26])[CH2:18][CH2:17]4)(O)[C:11]=1[C:10]=23.C(N(S(F)(F)[F:37])CC)C.C(=O)(O)[O-].[Na+]>ClCCl>[F:1][C:2]1[CH:3]=[N:4][C:5]2[CH:6]=[CH:7][C:8](=[O:30])[N:9]3[CH2:13][C:12]([CH2:15][N:16]4[CH2:21][CH2:20][CH:19]([NH:22][C:23](=[O:29])[O:24][C:25]([CH3:28])([CH3:27])[CH3:26])[CH2:18][CH2:17]4)([F:37])[C:11]=1[C:10]=23참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
A solution of 1,1-dimethylethyl {1-[(3-fluoro-4-hydroxy-7-oxo-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-4-yl)methyl]-4-piperidinyl}carbamate (15.93 g, 38.1 mmol) in dichloromethane (320 ml) was cooled in an ice bath and treated with (diethylamino)sulphur trifluoride (10.1 ml, 75.9 mmol). After 2.5 hours at room temperature saturated aqueous sodium bicarbonate solution was added, then the phases separated. The aqueous phase was extracted twice more with dichloromethane and the combined organic extracts combined and evaporated. Chromatography eluting with a methanol in dichloromethane gradient afforded the product (5.35 g, 33%).
후처리
- customthe phases separated
- extractionThe aqueous phase was extracted twice more with dichloromethane
- customevaporated
- washChromatography eluting with a methanol in dichloromethane gradient
출처 및 근거
- ORD 기록
- ord-a6eb2262d44f41418bb48bf5677e3a15
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07732460B2
연결된 노트
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