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Potassium tert-butoxide → 6-bromo-4-fluoro-1-isopropyl-2-methyl-1H-benzo(d)imidazole

HRID 2264373
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인쇄 미리보기

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HRID 2264373 반응식
CC(C)([O-])C.[K+].[Br:7][C:8]1[CH:13]=[C:12]([F:14])[C:11]([NH:15][C:16](=[N:18][CH:19]([CH3:21])[CH3:20])[CH3:17])=[C:10](F)[CH:9]=1>CNC=O>[Br:7][C:8]1[CH:13]=[C:12]([F:14])[C:11]2[N:15]=[C:16]([CH3:17])[N:18]([CH:19]([CH3:21])[CH3:20])[C:10]=2[CH:9]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 23665647Potassium tert-butoxideHCID 674267372177297-18-4

생성물 1

HCID 569716626-bromo-4-fluoro-1-isopropyl-2-methyl-1H-benzo(d)imidazole수율 72.9%

시약·촉매·용매 1

HCID 31254N-Methylformamide용매

반응 조건

온도
30 °C

실험 절차

Add potassium tert-butoxide (6.9 kg) in portions to a solution of N-(4-bromo-2,6-difluoro-phenyl)-N′-isopropyl-acetamidine (16.2 kg) in N-methyl formamide (76 kg) while maintaining the temperature at T<30° C. Heat the mixture at 70-75° C. until complete by HPLC. Cool to 20-30° C. and quench by adding into water (227 kg) then extract with MtBE (37×4 kg). Wash the combined organic phases with brine (49×2 kg) and concentrate to 25-30 L, add n-hexane (64 kg) and filter the slurry to give 11 kg of the title compound. MS (ES+): m/z=272 (M+H)+.

후처리

  1. temperatureHeat the mixture at 70-75° C. until complete by HPLC
  2. temperatureCool to 20-30° C.
  3. customquench
  4. additionby adding into water (227 kg)
  5. extractionthen extract with MtBE (37×4 kg)
  6. washWash the combined organic phases with brine (49×2 kg)
  7. concentrationconcentrate to 25-30 L
  8. additionadd n-hexane (64 kg)
  9. filtrationfilter the slurry

출처 및 근거

ORD 기록
ord-521327eff4b242749b88a137212eb609
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07855211B2

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