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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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methyl 1-methyl-3-nitro-1H-pyrazole-5-carboxylate → methyl 3-amino-1-methyl-1H-pyrazole-5-carboxylate

HRID 1918836
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인쇄 미리보기

반응식

HRID 1918836 반응식
[CH3:1][N:2]1[C:6]([C:7]([O:9][CH3:10])=[O:8])=[CH:5][C:4]([N+:11]([O-])=O)=[N:3]1.[H][H]>C(OCC)(=O)C.C(O)C.[Pd]>[NH2:11][C:4]1[CH:5]=[C:6]([C:7]([O:9][CH3:10])=[O:8])[N:2]([CH3:1])[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 18916504methyl 1-methyl-3-nitro-1H-pyrazole-5-carboxylateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 13248993methyl 3-amino-1-methyl-1H-pyrazole-5-carboxylate수율 100%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 702Ethanol용매HCID 8857Ethyl Acetate용매

실험 절차

In a 250 mL Parr hydrogenation flask was placed methyl 1-methyl-3-nitro-1H-pyrazole-5-carboxylate, (530 mg, 2.9 mmol) dissolved in ethyl acetate (15 mL) and ethanol (15 mL), to which was added 10% Pd/C (Degussa type) (100 mg). The mixture was placed on the Parr apparatus and pressurized with hydrogen to 50 PSI and shaken for 2.5 hrs. The reaction was filtered through a pad of celite which was washed with ethyl acetate. The solvent was removed under vacuum to give 119a as a white solid (450 mg, 2.9 mmol, quantitative yield).

후처리

  1. filtrationThe reaction was filtered through a pad of celite which
  2. washwas washed with ethyl acetate
  3. customThe solvent was removed under vacuum

출처 및 근거

ORD 기록
ord-2e6840a07b754b02bda836f48042426f
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08618107B2

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