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Ammonium formate → Ethyl 8-aminoquinoline-3-carboxylate

HRID 1531688
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반응식

HRID 1531688 반응식
C([O-])=O.[NH4+].Cl[C:6]1[C:15]2[C:10](=[C:11]([N+:16]([O-])=O)[CH:12]=[CH:13][CH:14]=2)[N:9]=[CH:8][C:7]=1[C:19]([O:21][CH2:22][CH3:23])=[O:20]>[Pd].C(O)C>[CH2:22]([O:21][C:19]([C:7]1[CH:8]=[N:9][C:10]2[C:15]([CH:6]=1)=[CH:14][CH:13]=[CH:12][C:11]=2[NH2:16])=[O:20])[CH3:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 2723923Ammonium formateHCID 11196760Ethyl 4-chloro-8-nitroquinoline-3-carboxylate

생성물 1

HCID 21250128Ethyl 8-aminoquinoline-3-carboxylate수율 58%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

Ammonium formate was added to a vigorously stirred mixture of 4-chloro-3-ethoxycarbonyl-8-nitro-quinoline (5.6 g), ethanol (1000 ml) and 10% palladium on carbon catalyst (2 g). The mixture was stirred at ambient temperature for 1 hour, filtered through a pad of celite and the pad washed with dichloromethane. The combined filtrate and washings were evaporated to dryness. The residue so obtained was purified by flash chromatography on silica using chloroform as eluant to give 3-ethoxycarbonyl-8-amino-quinoline in 58% yield, mp 94-96° C.

후처리

  1. filtrationfiltered through a pad of celite
  2. washthe pad washed with dichloromethane
  3. customThe combined filtrate and washings were evaporated to dryness
  4. customThe residue so obtained
  5. customwas purified by flash chromatography on silica

출처 및 근거

ORD 기록
ord-721f8a81d01b4203b75e626acbda4ef5
출처 데이터셋
uspto-grants-2001_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06200974B1

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