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HCID 4137682, 화합물 → 5-Benzoxazolamine, 2-(3-aminophenyl)-

HRID 325088
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인쇄 미리보기

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HRID 325088 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([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:7]=[CH:8][CH:9]=1)([O-])=O>C(O)CC.[Pd]>[NH2:1][C:4]1[CH:5]=[C:6]([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:7]=[CH:8][CH:9]=1
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참가 물질

4

반응물 1

HCID 4137682HCID 4137682, 화합물

생성물 1

HCID 7625455-Benzoxazolamine, 2-(3-aminophenyl)-

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 10311-Propanol용매

반응 조건

온도
70 °C

실험 절차

A 11.1-gram portion of the 2-(m-nitrophenyl)-5-nitrobenzoxazole is dissolved in 200 milliliters of n-propanol. A 10% palladium-on-carbon catalyst (2.0 grams) is added, and the mixture stirred under nitrogen. The mixture is heated to 70° C., and hydrogen gas is bubbled into the mixture until substantially all the nitro groups have been reduced to primary amine groups, as indicated by liquid chromatography. The catalyst is then filtered off and the remaining solution added to water. The solvent and water are then evaporated off to yield 2-(m-aminophenyl)-5-aminobenzoxazole.

후처리

  1. customhydrogen gas is bubbled into the mixture until substantially all the nitro groups
  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-769ea3da9059411597f6f74131294edb
출처 데이터셋
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06222044B1

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