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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trimethylsilyldiazomethane → methyl 1H-indazole-4-carboxylate

HRID 1677676
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HRID 1677676 반응식
[NH:1]1[C:9]2[CH:8]=[CH:7][CH:6]=[C:5]([C:10]([OH:12])=[O:11])[C:4]=2[CH:3]=[N:2]1.[CH3:13][Si](C=[N+]=[N-])(C)C>CO.C1(C)C=CC=CC=1>[CH3:13][O:11][C:10]([C:5]1[C:4]2[CH:3]=[N:2][NH:1][C:9]=2[CH:8]=[CH:7][CH:6]=1)=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 167693TrimethylsilyldiazomethaneHCID 219823231H-indazole-4-carboxylic acid

생성물 1

HCID 6623327methyl 1H-indazole-4-carboxylate

시약·촉매·용매 2

HCID 887Methanol용매HCID 1140Toluene용매2회

실험 절차

Indazole-4-carboxylic acid (2.00 g, 12.3 mmol) was suspended in methanol (20 mL) and toluene (30 mL) at room temperature. A solution of 2 M trimethylsilyl diazomethane (12 mL, 24 mmol) in toluene was added slowly and the mixture was stirred at room temperature until the solution turned yellow. The reaction was quenched with concentrated acetic acid (5 mL) and the solvent was removed in vacuo. The residue was purified by silica gel chromatography eluting with a gradient of 0-30% ethyl acetate in hexanes to afford 1H-indazole-4-carboxylic acid methyl ester.

후처리

  1. customat room temperature
  2. customThe reaction was quenched with concentrated acetic acid (5 mL)
  3. customthe solvent was removed in vacuo
  4. customThe residue was purified by silica gel chromatography
  5. washeluting with a gradient of 0-30% ethyl acetate in hexanes

출처 및 근거

ORD 기록
ord-66a90aa1743c45c0a9153fc1c03ce5ba
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08008327B2

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