Hydrochloric Acid → Ethyl 4-[1-(4-chlorobenzyl)-5-fluorobenzimidazol-2-yl]-3,3-dimethylbutanoate

HRID 653668Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 653668
[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([CH2:6][NH:7][C:8]2[CH:14]=[CH:13][C:12]([F:15])=[CH:11][C:9]=2[NH2:10])=[CH:4][CH:3]=1.[CH3:18][CH:19]=C(C)C.[CH3:23][C:24]([CH3:33])([CH2:29][C:30](O)=O)[CH2:25][C:26]([OH:28])=[O:27].Cl>C(Cl)(Cl)Cl.C(O)C.C(N(CC)CC)C>[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([CH2:6][N:7]2[C:8]3[CH:14]=[CH:13][C:12]([F:15])=[CH:11][C:9]=3[N:10]=[C:30]2[CH2:29][C:24]([CH3:23])([CH3:33])[CH2:25][C:26]([O:28][CH2:18][CH3:19])=[O:27])=[CH:4][CH:3]=1

Komponenten

8

Edukt 4

HCID 313Hydrochloric AcidHCID 105532-Methyl-2-butene2×HCID 209843,3-Dimethylglutaric acidHCID 149529912-(4-Chlorobenzylamino)-5-fluoroaniline

Produkt 1

HCID 14953020Ethyl 4-[1-(4-chlorobenzyl)-5-fluorobenzimidazol-2-yl]-3,3-dimethylbutanoate

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 702EthanolLösungsmittelHCID 6212ChloroformLösungsmittel2×HCID 8471TriethylamineLösungsmittel

Versuchsvorschrift

10 g of 2-(4-chlorobenzylamino)-5-fluoroaniline, prepared in Example 8, are dissolved in 100 ml of chloroform, stabilized with amylene, and 6 ml of triethylamine. A solution of 8.25 g of the acid chloride ethyl ester of 3,3-dimethylglutaric acid, prepared in Example 28, in 20 ml of chloroform, stabilized with amylene, is added dropwise. The mixture is stirred for two hours at room temperature, the crystals formed are filtered off and the solvents are evaporated off under vacuum. The residue obtained is dissolved in 200 ml of ethanol and 30 ml of concentrated hydrochloric acid and the mixture is refluxed for 10 hours. The solvents are evaporated off to dryness and the residue is taken up with water and then extracted with ethyl acetate. The organic phase is dried and evaporated under vacuum to give 14 g of ethyl 4-[1-(4-chlorobenzyl)-5-fluorobenzimidazol-2-yl]-3,3-dimethylbutanoate in the form of an oil, which is used as such for the next step.

Aufarbeitung

  1. additionis added dropwise
  2. customthe crystals formed
  3. filtrationare filtered off
  4. customthe solvents are evaporated off under vacuum
  5. customThe residue obtained
  6. customThe solvents are evaporated off to dryness
  7. extractionextracted with ethyl acetate
  8. customThe organic phase is dried
  9. customevaporated under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-fc8b5d242c1a49178f469351a9e8646c
Quelldatensatz
uspto-grants-1992_07
Patentnummer
US05128359

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