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

HRID 353815Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 353815
[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

Komponenten

6

Edukt 4

HCID 962WaterHCID 24758Sodium hydrideHCID 256687Methyl 4-(bromomethyl)benzoateHCID 69918962-(Pyrrolidin-1-yl)-1H-benzo[d]imidazole

Produkt 1

HCID 12144533methyl 4-[(2-pyrrolidinyl-1H-benzimidazol-1yl)methyl]benzoate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

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. Analysis: Calculated for C20H21N3O2: % C, 71.62; % H, 6.31; % N, 12.53. Found: % C, 71.44; % H, 6.41; % N, 12.50.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-3f646bc23b97451a909f1edd272f55d1
Quelldatensatz
uspto-grants-2004_06
Patentnummer
US06756382B2

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