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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → 1H-Isoindol-1-one, 4-bromo-2,3-dihydro-7-methoxy-

HRID 1247457
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HRID 1247457 반응식
[Br:1][C:2]1[CH:10]=[CH:9][C:8]([OH:11])=[C:7]2[C:3]=1[CH2:4][NH:5][C:6]2=[O:12].[C:13]([O-])([O-])=O.[Cs+].[Cs+].CI.O>CN(C=O)C>[Br:1][C:2]1[CH:10]=[CH:9][C:8]([O:11][CH3:13])=[C:7]2[C:3]=1[CH2:4][NH:5][C:6]2=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 6328Methyl iodideHCID 10796Cesium carbonateHCID 219075534-Bromo-7-hydroxyisoindolin-1-one

생성물 1

HCID 219075551H-Isoindol-1-one, 4-bromo-2,3-dihydro-7-methoxy-수율 70%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A solution of Example 106D (103 mg, 0.45 mmol) in DMF (4 mL) was treated with Cs2CO3 (162 mg, 0.5 mmol) and methyl iodide (0.03 mL, 0.48 mmol), stirred at room temperature for 3 hours, then poured into water. The resulting precipitate was filtered to give 76 mg (70%) of the desired product. MS (ESI(+)) m/e 242,244 (M+H)+.

후처리

  1. filtrationThe resulting precipitate was filtered

출처 및 근거

ORD 기록
ord-26983ef7633a4dfd8fe5b31dd29a466a
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07129260B2

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