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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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5-Nitro-3-isoquinolinecarboxylic acid → 5-Aminoisoquinoline-3-carboxylic acid

HRID 1902550
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반응식

HRID 1902550 반응식
[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[C:7]([C:14]([OH:16])=[O:15])[N:8]=[CH:9]2)([O-])=O>CO.[Pd]>[NH2:1][C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[C:7]([C:14]([OH:16])=[O:15])[N:8]=[CH:9]2
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참가 물질

4

반응물 1

HCID 193906095-Nitro-3-isoquinolinecarboxylic acid

생성물 1

HCID 205156525-Aminoisoquinoline-3-carboxylic acid수율 92.2%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

5-Nitroisoquinoline-3-carboxylic acid (44 g) is dissolved in methanol (3 liters), and a catalyst consisting of palladium-on-carbon (3/97 by weight; 15 g) is added. The mixture is hydrogenated at atmospheric pressure, at a temperature between 20° and 25° C. After stirring for 5 hours, the volume of hydrogen absorbed is 13.9 liters. The mixture is filtered through diatomaceous silica and the filtrate is concentrated to dryness under reduced pressure (20 mm Hg; 2.7 kPa) at 60° C. to yield 5-aminoisoquinoline-3-carboxylic acid (35 g).

후처리

  1. additionis added
  2. customis hydrogenated at atmospheric pressure, at a temperature between 20° and 25° C
  3. customthe volume of hydrogen absorbed
  4. filtrationThe mixture is filtered through diatomaceous silica
  5. concentrationthe filtrate is concentrated to dryness under reduced pressure (20 mm Hg; 2.7 kPa) at 60° C.

출처 및 근거

ORD 기록
ord-f408aa0ee97740cc8926906d0cd84de3
출처 데이터셋
uspto-grants-1982_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04363909

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