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Ethanol → 2-[-5,6-Dimethoxy-2-1H-benzimidazolylthio]-4-methoxy benzenamine

HRID 1199461
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HRID 1199461 반응식
[CH3:1][O:2][C:3]1[C:23]([O:24][CH3:25])=[CH:22][C:6]2[NH:7][C:8]([S:10][C:11]3[CH:16]=[C:15]([O:17][CH3:18])[CH:14]=[CH:13][C:12]=3[N+:19]([O-])=O)=[N:9][C:5]=2[CH:4]=1.[Cl-].[NH4+].C(O)C.O>[Fe].CCOCC>[CH3:1][O:2][C:3]1[C:23]([O:24][CH3:25])=[CH:22][C:6]2[NH:7][C:8]([S:10][C:11]3[CH:16]=[C:15]([O:17][CH3:18])[CH:14]=[CH:13][C:12]=3[NH2:19])=[N:9][C:5]=2[CH:4]=1
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참가 물질

7

반응물 4

HCID 702EthanolHCID 962WaterHCID 25517Ammonium ChlorideHCID 198667335,6-Dimethoxy-2-(5-methoxy-2-nitrophenylthio)-1H-benzimidazole

생성물 1

HCID 198667012-[-5,6-Dimethoxy-2-1H-benzimidazolylthio]-4-methoxy benzenamine

시약·촉매·용매 2

HCID 23925Iron촉매
HCID 3283Diethyl Ether용매

실험 절차

The product of step (a) above (6.3 g), iron powder (6.3 g) and ammonium chloride (6.3 g) were stirred together with ethanol (63 ml) and water (120 ml) and heated under reflux for 1 hour. The hot mixture was filtered and the residue washed with hot ethyl acetate (500 ml). The combined filtrates were separated and the aqueous phase extracted with ethyl acetate. The combined ethyl acetate extracts were washed with water and brine, then dried and evaporated to leave a foam. Upon trituration with ether the sub-title compound was formed as a grey solid, MS MW bp 331.

후처리

  1. temperatureheated
  2. temperatureunder reflux for 1 hour
  3. filtrationThe hot mixture was filtered
  4. washthe residue washed with hot ethyl acetate (500 ml)
  5. customThe combined filtrates were separated
  6. extractionthe aqueous phase extracted with ethyl acetate
  7. washThe combined ethyl acetate extracts were washed with water and brine
  8. customdried
  9. customevaporated
  10. customto leave a foam

출처 및 근거

ORD 기록
ord-0b4a3e604c3a49be8057c4f868650ba0
출처 데이터셋
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04900751

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