Water → methyl 4-[(2-pyrrolidinyl-1H-benzimidazol-1yl)methyl]benzoate

HRID 746499노트

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HRID 746499 반응식
[H-].[Na+].[N:3]1([C:8]2[NH:12][C:11]3[CH:13]=[CH:14][CH:15]=[CH:16][C:10]=3[N:9]=2)[CH2:7][CH2:6][CH2:5][CH2:4]1.Br[CH2:18][C:19]1[CH:28]=[CH:27][C:22]([C:23]([O:25][CH3:26])=[O:24])=[CH:21][CH:20]=1.O>CN(C)C=O>[N:3]1([C:8]2[N:9]([CH2:18][C:19]3[CH:28]=[CH:27][C:22]([C:23]([O:25][CH3:26])=[O:24])=[CH:21][CH:20]=3)[C:10]3[CH:16]=[CH:15][CH:14]=[CH:13][C:11]=3[N:12]=2)[CH2:7][CH2:6][CH2:5][CH2:4]1

참가 물질

6

실험 절차

Sodium hydride (402 mg, 11 mmol) was added to a suspension of 2-pyrrolidino-1H-benzimidazole (1.9 g, 10.1 mmol) in dry N,N-dimethylformamide (30 mL). All solids dissolved. The solution was allowed to stir at ambient temperature for 15 minutes following the cessation of foaming. The solution was cooled to 5° C. and a solid formed. Methyl 4-(bromomethyl)benzoate (2.1 g, 01 mol) was added to the suspension and all the solids dissolved. The solution was allowed to stir at ambient temperature and a solid formed. The mixture was stirred at ambient temperature overnight and then it was poured into cold water. A solid was isolated by filtration, washed with water and dried to provide 3.0 g of crude product as an off-white solid. This material was recrystallized from methanol to provide methyl 4-[(2-pyrrolidinyl-1H-benzimidazol-1yl)methyl]benzoate.

후처리

  1. dissolutionAll solids dissolved
  2. temperatureThe solution was cooled to 5° C.
  3. customa solid formed
  4. dissolutiondissolved
  5. stirringto stir at ambient temperature
  6. customa solid formed
  7. stirringThe mixture was stirred at ambient temperature overnight
  8. customA solid was isolated by filtration
  9. washwashed with water
  10. customdried
  11. customto provide 3.0 g of crude product as an off-white solid
  12. customThis material was recrystallized from methanol

출처 및 근거

ORD 기록
ord-123f12732da949de86dcb7e1077db460
출처 데이터셋
uspto-grants-2008_07
특허 번호
US07393859B2

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