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1-(2,3-Dihydro-5-nitro-1H-pyrrolo(2,3-b)pyridin-1-yl)ethanone → HCID 66845730, 화합물

HRID 1804736
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인쇄 미리보기

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HRID 1804736 반응식
[C:1]([N:4]1[C:8]2=[N:9][CH:10]=[C:11]([N+:13]([O-])=O)[CH:12]=[C:7]2[CH2:6][CH2:5]1)(=[O:3])[CH3:2].[H][H]>C(O)C.[Pd]>[C:1]([N:4]1[C:8]2=[N:9][CH:10]=[C:11]([NH2:13])[CH:12]=[C:7]2[CH2:6][CH2:5]1)(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 137785751-(2,3-Dihydro-5-nitro-1H-pyrrolo(2,3-b)pyridin-1-yl)ethanoneHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 66845730HCID 66845730, 화합물수율 65.1%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A suspension of 0.43 g (2.08 mmol) of 1-acetyl-2,3-dihydro-5-nitro-1H-pyrrolo[2,3-b]pyridine (Tetrahedron Lett. 1987, 1589) and 0.044 g of 10% palladium-on-charcoal in 15 mL of ethanol is stirred vigorously for 6 hours at room temperature and under 5 atmospheres of hydrogen. After this time, the suspension is filtered through Celite and the filtrate is concentrated under reduced pressure to give 0.24 g of the expected product in the form of a solid.

후처리

  1. filtrationAfter this time, the suspension is filtered through Celite
  2. concentrationthe filtrate is concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-c1d594c5907041dcb4d7bebf8c60051c
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08354425B2

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