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Acetic Acid → 5-(Benzoxazol-2-yl)-1-(2-(methylthio)ethyl)-2-methylbenzimidazole

HRID 74313
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HRID 74313 반응식
[CH3:1][S:2][CH2:3][CH2:4][NH:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[O:13][C:14]3[CH:20]=[CH:19][CH:18]=[CH:17][C:15]=3[N:16]=2)=[CH:8][C:7]=1[N+:21]([O-])=O.[C:24](O)(=O)[CH3:25]>[Fe]>[O:13]1[C:14]2[CH:20]=[CH:19][CH:18]=[CH:17][C:15]=2[N:16]=[C:12]1[C:9]1[CH:10]=[CH:11][C:6]2[N:5]([CH2:4][CH2:3][S:2][CH3:1])[C:24]([CH3:25])=[N:21][C:7]=2[CH:8]=1
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참가 물질

4

반응물 2

HCID 176Acetic AcidHCID 67498515N-(2-(methylthio)ethyl)-4-(benzoxazol-2-yl)-2-nitroaniline

생성물 1

HCID 674980175-(Benzoxazol-2-yl)-1-(2-(methylthio)ethyl)-2-methylbenzimidazole수율 84%

시약·촉매·용매 1

HCID 23925Iron촉매

실험 절차

To N-(2-(methylthio)ethyl)-4-(benzoxazol-2-yl)-2-nitroaniline (370 mg, 1.12 mmol) was added iron powder (188 mg, 3.37 mmol) and acetic acid (5 mL), and this was heated to reflux for 10 hours. After the reaction solution was cooled, it was concentrated. The residue obtained was purified by silica gel column chromatography to yield the title compound (305 mg, 84% yield) as pink crystals.

후처리

  1. temperaturethis was heated
  2. temperatureto reflux for 10 hours
  3. temperatureAfter the reaction solution was cooled
  4. concentrationit was concentrated
  5. customThe residue obtained
  6. customwas purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-08b3d63d714e4b7fbf514d8a143b8fd6
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08829035B2

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