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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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6-(Cyclohexylamino)-5-nitropyridin-2-yl methanesulfonate → 5-Amino-6-(cyclohexylamino)pyridin-2-yl Methanesulfonate

HRID 1890356
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인쇄 미리보기

반응식

HRID 1890356 반응식
[CH3:1][S:2]([O:5][C:6]1[CH:11]=[CH:10][C:9]([N+:12]([O-])=O)=[C:8]([NH:15][CH:16]2[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]2)[N:7]=1)(=[O:4])=[O:3]>CO.[Pd]>[CH3:1][S:2]([O:5][C:6]1[CH:11]=[CH:10][C:9]([NH2:12])=[C:8]([NH:15][CH:16]2[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21]2)[N:7]=1)(=[O:3])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 866552596-(Cyclohexylamino)-5-nitropyridin-2-yl methanesulfonate

생성물 1

HCID 866552605-Amino-6-(cyclohexylamino)pyridin-2-yl Methanesulfonate

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

6-(Cyclohexylamino)-5-nitropyridin-2-yl methanesulfonate (1.58 g, 5.01 mmol) was dissolved in methanol (1000 mL). Palladium (5% Pd/C, 1.72 g, 0.075 mmol) was added. The reaction was flushed with nitrogen and stirred under a balloon filled with hydrogen over 3 h at room temperature. The mixture was filtered through Celite® and concentrated to give the title compound as a dark green solid which was used immediately in next step without further purification.

후처리

  1. customThe reaction was flushed with nitrogen
  2. additionfilled with hydrogen over 3 h at room temperature
  3. filtrationThe mixture was filtered through Celite®
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-2a66edd8cc914e92bdf57fb88b254619
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08507473B2

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