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Cesium fluoride → 1-Fluoro-4-(2-methoxyethoxy)isoquinoline

HRID 1852132
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HRID 1852132 반응식
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([O:12][CH2:13][CH2:14][O:15][CH3:16])=[CH:4][N:3]=1.[F-:17].[Cs+]>CS(C)=O>[F:17][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([O:12][CH2:13][CH2:14][O:15][CH3:16])=[CH:4][N:3]=1
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참가 물질

4

반응물 2

HCID 25953Cesium fluorideHCID 86683208HCID 86683208, 화합물

생성물 1

HCID 709782881-Fluoro-4-(2-methoxyethoxy)isoquinoline

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

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온도
140 °C

실험 절차

To a solution of 1-chloro-4-(2-methoxyethoxy)isoquinoline (368 mg, 1.548 mmol) in DMSO (7 mL) was added CsF (470 mg, 3.10 mmol) and heated to 140° C. for 2 hrs. LC/MS showed the desired product. The reaction was diluted with Ethylacteate and washed with water, and brine. The organic phase was collected, dried over sodium sulfate, and concentrated under vacuum to give the crude product which was purified by silica gel chromatography using a gradient of 5-25% EtOAc/Hexanes. The product fractions were collected and the solvent removed under vacuum to give it the desired product 1-fluoro-4-(2-methoxyethoxy)isoquinoline (241 mg, 70.4% yield) as a white solid. MS: MS m/z 222.15 (M++1).

출처 및 근거

ORD 기록
ord-6ef9b9e6c4e94ae5a61251631762d6ee
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08957203B2

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