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2-Methoxy-3-nitro-5-ethyl-6-methylpyridine → 2-Methoxy-3-amino-5-ethyl-6-methylpyridine

HRID 1033006
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인쇄 미리보기

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HRID 1033006 반응식
[CH3:1][O:2][C:3]1[C:8]([N+:9]([O-])=O)=[CH:7][C:6]([CH2:12][CH3:13])=[C:5]([CH3:14])[N:4]=1>CO.O1CCCC1.[Pd]>[CH3:1][O:2][C:3]1[C:8]([NH2:9])=[CH:7][C:6]([CH2:12][CH3:13])=[C:5]([CH3:14])[N:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 104652702-Methoxy-3-nitro-5-ethyl-6-methylpyridine

생성물 1

HCID 103747942-Methoxy-3-amino-5-ethyl-6-methylpyridine수율 98%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 887Methanol용매HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 2-methoxy-3-nitro-5-ethyl-6-methylpyridine (535 mg, 2.72 mmol) in methanol (8 mL) and tetrahydrofuran (8 mL) containing 5% palladium on carbon (83 mg) was hydrogenated at atmospheric pressure for 5 hours. The catalyst was filtered off the solvent evaporated to yield 436 mg (98%) of oily product.

후처리

  1. filtrationThe catalyst was filtered off the solvent
  2. customevaporated

출처 및 근거

ORD 기록
ord-43607c74710f483782df876a5943b4f2
출처 데이터셋
uspto-grants-1994_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05308854

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