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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Methanol → HCID 178486902, 화합물

HRID 2391740
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HRID 2391740 반응식
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([NH2:9])[C:6]([N+:10]([O-])=O)=[CH:5][N:4]=1.[CH3:13]O>[Pd]>[CH3:1][O:2][C:3]1[N:4]=[CH:5][C:6]2[N:10]=[CH:13][NH:9][C:7]=2[CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 887MethanolHCID 147626984-Amino-2-methoxy-5-nitropyridine

생성물 1

HCID 178486902HCID 178486902, 화합물

시약·촉매·용매 1

HCID 23938Palladium촉매

실험 절차

A solution of 15.51 g of 2-methoxy-5-nitropyridin-4-amine (example E7) in 1.55 I methanol was treated with 4.65 g Pd/C (10% Pd) and hydrogenated for 12 h under atmospheric pressure. The reaction mixture was filtered through a plug of CELITE® (diatomaceous earth) and the filtrate was concentrated under vacuum. The resulting residue was treated with 181 ml formic acid and the mixture was refluxed for 50 h. The formic acid was distilled off and the residue was repeatedly purified by flash chromatography (neutral alumina oxide, ethyl acetate/methanol) to yield the title compound.

후처리

  1. filtrationThe reaction mixture was filtered through a plug of CELITE® (diatomaceous earth)
  2. concentrationthe filtrate was concentrated under vacuum
  3. additionThe resulting residue was treated with 181 ml formic acid
  4. temperaturethe mixture was refluxed for 50 h
  5. distillationThe formic acid was distilled off
  6. customthe residue was repeatedly purified by flash chromatography (neutral alumina oxide, ethyl acetate/methanol)

출처 및 근거

ORD 기록
ord-27bcb2a5bc1c4039ac9641ce91c8049e
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08273890B2

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