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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Carbon Dioxide → 7-Fluoro-1H-indole-5-carboxylic acid

HRID 468197
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HRID 468197 반응식
Br[C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([F:11])[CH:10]=1)[NH:7][CH:6]=[CH:5]2.[Li]CCCC.[C:17](=[O:19])=[O:18].O>C1COCC1>[F:11][C:9]1[CH:10]=[C:2]([C:17]([OH:19])=[O:18])[CH:3]=[C:4]2[C:8]=1[NH:7][CH:6]=[CH:5]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 280Carbon DioxideHCID 962WaterHCID 35348805-bromo-7-fluoro-1H-indoleHCID 178418339Butyllithium

생성물 1

HCID 115645587-Fluoro-1H-indole-5-carboxylic acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 5-bromo-7-fluoroindole 70f (1.71 mmol, 365 mg) in THF at −60° C. was added n-BuLi (1.6 M solution in hexanes, 5.2 mmol, 3.2 mL). The solution was kept at −60° C. for 4 h and was then poured onto an excess of freshly crushed dry ice. Water was added and the mixture was acidified to pH=4. The organic phase was concentrated and the residue was purified by flash column chromatography (silica gel, 35% EtOAc/hexanes) to give compound 70h.

후처리

  1. concentrationThe organic phase was concentrated
  2. customthe residue was purified by flash column chromatography (silica gel, 35% EtOAc/hexanes)
  3. customto give compound 70h.

출처 및 근거

ORD 기록
ord-8789c10a7a45468d99f6394b640037d2
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08623858B2

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