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5-Nitro-2,3-diphenylpyridine → 5,6-Diphenylpyridin-3-amine

HRID 41988
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인쇄 미리보기

반응식

HRID 41988 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[C:7]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[N:8][CH:9]=1)([O-])=O>CO.[Pd]>[C:16]1([C:6]2[CH:5]=[C:4]([NH2:1])[CH:9]=[N:8][C:7]=2[C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 673943515-Nitro-2,3-diphenylpyridine

생성물 1

HCID 584158885,6-Diphenylpyridin-3-amine

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

A mixture of 5-nitro-2,3-diphenylpyridine (0.74 mmol, 0.21 g) and Pd/C 10% (0.02 g) in methanol (5 ml) was stirred for 16 hours under hydrogen atmosphere. The catalyst was filtered off and the solid thoughtfully washed with methanol. The solid residue was purified by chromatography over SiO2 eluting with hexane/ethyl acetate mixtures affording 0.14 g (74% of yield) of the expected product.

후처리

  1. filtrationThe catalyst was filtered off
  2. washthe solid thoughtfully washed with methanol
  3. customThe solid residue was purified by chromatography over SiO2 eluting with hexane/ethyl acetate
  4. custommixtures affording

출처 및 근거

ORD 기록
ord-11f155da721a4d2686ce16e3395a406e
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08536165B2

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