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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 19002930, 화합물 → HCID 19002888, 화합물

HRID 2259508
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HRID 2259508 반응식
Cl[C:2]1[O:10][C:9]2[C:4](=[N:5][C:6]([CH3:11])=[CH:7][CH:8]=2)[C:3]=1[Cl:12].C([Li])(C)(C)C>C1COCC1>[Cl:12][C:3]1[C:4]2=[N:5][C:6]([CH3:11])=[CH:7][CH:8]=[C:9]2[O:10][CH:2]=1
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참가 물질

4

반응물 2

HCID 19002930HCID 19002930, 화합물HCID 178418306HCID 178418306, 화합물

생성물 1

HCID 19002888HCID 19002888, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 2,3-dichloro-5-methylfuro[3,2-b]pyridine (0.661 g, 3.27 mmol) (Example 12, Step 2) in 16 mL of THF was added a 1.7M solution of t-butyllithium (4.04 mL, 6.87 mmol). After 30 min the solution was quenched at -78° C. with methanol and a solution of NH4C1. The reaction was brought to room temperature and extracted with EtOAc. The organic solvents were evaporated and the title compound was purified by flash chromatography on silica with EtOAc:hexane 1:4 to yield 0.444 g (81%).

후처리

  1. customAfter 30 min the solution was quenched at -78° C. with methanol
  2. customwas brought to room temperature
  3. extractionextracted with EtOAc
  4. customThe organic solvents were evaporated
  5. customthe title compound was purified by flash chromatography on silica with EtOAc:hexane 1:4
  6. customto yield 0.444 g (81%)

출처 및 근거

ORD 기록
ord-06347123ff744e688129a25fe29d93b1
출처 데이터셋
uspto-grants-1995_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05472964

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