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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Methyl 1-methyl-5-nitro-1H-pyrrole-2-carboxylate → Methyl 5-amino-1-methyl-1H-pyrrole-2-carboxylate

HRID 726477
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인쇄 미리보기

반응식

HRID 726477 반응식
[CH3:1][N:2]1[C:6]([N+:7]([O-])=O)=[CH:5][CH:4]=[C:3]1[C:10]([O:12][CH3:13])=[O:11]>[Pd].CO>[CH3:1][N:2]1[C:6]([NH2:7])=[CH:5][CH:4]=[C:3]1[C:10]([O:12][CH3:13])=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 14487173Methyl 1-methyl-5-nitro-1H-pyrrole-2-carboxylate

생성물 1

HCID 16085054Methyl 5-amino-1-methyl-1H-pyrrole-2-carboxylate

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

1.31 g (7.4 mmol) of methyl N-methyl-5-nitro-2-pyrrolecarboxylate, 400 mg of palladium on carbon (10%) and 50 ml of methanol were introduced into a reactor. The mixture was hydrogenated at room temperature and at a pressure of 7 bar for 2 hours. The catalyst was filtered, washed twice with 25 ml of methanol and the filtrates evaporated. 1.1 g (100%) of the expected amine was recovered in the form of a dark red oil.

후처리

  1. filtrationThe catalyst was filtered
  2. washwashed twice with 25 ml of methanol
  3. customthe filtrates evaporated
  4. custom1.1 g (100%) of the expected amine was recovered in the form of a dark red oil

출처 및 근거

ORD 기록
ord-240b193a74654233bc58222f2f2de360
출처 데이터셋
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05709867

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