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Trimethyl orthoacetate → 4-Bromo-6-chloro-2-methyl-1H-benzo[d]imidazole

HRID 475126
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HRID 475126 반응식
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([NH2:8])[C:3]=1[NH2:9].[Cl:10][Sn]Cl.CO[C:15](OC)(OC)[CH3:16]>CCO>[Br:1][C:2]1[C:3]2[N:9]=[C:15]([CH3:16])[NH:8][C:4]=2[CH:5]=[C:6]([Cl:10])[CH:7]=1
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참가 물질

5

반응물 3

HCID 15050Trimethyl orthoacetateHCID 24479Stannous ChlorideHCID 124898393-Bromobenzene-1,2-diamine

생성물 1

HCID 532168604-Bromo-6-chloro-2-methyl-1H-benzo[d]imidazole수율 89.7%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A suspension of 3-bromobenzene-1,2-diamine (4.0 g, 15.90 mmol) and SnCl2 (17.9 g, 79.50 mmol) in EtOH (40 mL) was heated at reflux for 4 h. After cooling to RT, 1,1,1-trimethoxyethane (12.9 g, 79.50 mmol) was added. The reaction mixture was stirred at 120° C. for 14 h, cooled to RT and concentrated in vacuo. The residue was diluted with EtOAc (100 mL), treated with saturated NaHCO3 solution (200 mL), filtered through Celite®, and washed with EtOAc (50 mL×3). The filtrate was washed with saturated NaHCO3, water, and brine, dried (MgSO4), filtered, and concentrated in vacuo to afford 4-bromo-6-chloro-2-methyl-1H-benzo[d]imidazole as a yellow solid (3.5 g, 89.7%). MS (ESI): m/z=244.9 [M+1]+.

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 4 h
  3. temperaturecooled to RT
  4. concentrationconcentrated in vacuo
  5. additionThe residue was diluted with EtOAc (100 mL)
  6. additiontreated with saturated NaHCO3 solution (200 mL)
  7. filtrationfiltered through Celite®
  8. washwashed with EtOAc (50 mL×3)
  9. washThe filtrate was washed with saturated NaHCO3, water, and brine
  10. dry with materialdried (MgSO4)
  11. filtrationfiltered
  12. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-89c01840eab34a529b759de7f5157770
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08637537B2

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