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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Cesium fluoride → 3-Methoxyquinoxalin-5-ol

HRID 1437375
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HRID 1437375 반응식
[CH3:1][O:2][C:3]1[CH:12]=[N:11][C:10]2[C:5](=[C:6]([O:13][Si](C(C)C)(C(C)C)C(C)C)[CH:7]=[CH:8][CH:9]=2)[N:4]=1.[F-].[Cs+]>O1CCCC1.CO>[CH3:1][O:2][C:3]1[CH:12]=[N:11][C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([OH:13])[C:5]=2[N:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 25953Cesium fluorideHCID 686959212-Methoxy-8-triisopropylsilanyloxy-quinoxaline

생성물 1

HCID 1362623933-Methoxyquinoxalin-5-ol수율 113.5%

시약·촉매·용매 1

HCID 21899815MeOH tetrahydrofuran용매

실험 절차

A solution of (d) (6.95 g, 21 mmol) in tetrahydrofuran/methanol (280 ml/140 ml) was treated with caesium fluoride (4.73 g, 31.4 mmol) and stirred for 18 hours. The mixture was evaporated and the residue partitioned between diethyl ether and dilute aqueous hydrochloric acid. The aqueous phase was further extracted with diethyl ether and the combined extracts dried and evaporated to give an oil (4.2 g).

후처리

  1. customThe mixture was evaporated
  2. customthe residue partitioned between diethyl ether and dilute aqueous hydrochloric acid
  3. extractionThe aqueous phase was further extracted with diethyl ether
  4. customthe combined extracts dried
  5. customevaporated

출처 및 근거

ORD 기록
ord-e352872d5e004c98b4fdadc92c7b0840
출처 데이터셋
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07622481B2

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