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HCID 3089143, 화합물 → 2-(4-Aminophenyl)benzoxazol-5-amine

HRID 865814
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인쇄 미리보기

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HRID 865814 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[O:11][C:12]3[CH:18]=[CH:17][C:16]([N+:19]([O-])=O)=[CH:15][C:13]=3[N:14]=2)=[CH:6][CH:5]=1)([O-])=O>O1CCOCC1.[Pd]>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]([C:10]2[O:11][C:12]3[CH:18]=[CH:17][C:16]([NH2:19])=[CH:15][C:13]=3[N:14]=2)=[CH:8][CH:9]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 3089143HCID 3089143, 화합물

생성물 1

HCID 6143852-(4-Aminophenyl)benzoxazol-5-amine

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 312751,4-Dioxane용매

반응 조건

온도
53 °C

실험 절차

A 7.5-gram portion of the 2-(p-nitrophenyl)-5-nitrobenzoxazole is dissolved in 100 milliliters of 1,4-dioxane. A 10% palladium-on-carbon catalyst (2.0 grams) is added, and the mixture stirred under nitrogen. The mixture is heated to 53° C., and hydrogen gas is bubbled into the mixture for about 6.5 hours. The catalyst is then filtered off and the remaining solution added to water. The solvent and water are then evaporated off to yield 2-(p-aminophenyl)-5-aminobenzoxazole.

후처리

  1. customhydrogen gas is bubbled into the mixture for about 6.5 hours
  2. filtrationThe catalyst is then filtered off
  3. additionthe remaining solution added to water
  4. customThe solvent and water are then evaporated off

출처 및 근거

ORD 기록
ord-455e22da642a43a8ae3425956ca9bb0e
출처 데이터셋
uspto-grants-1996_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05567843

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