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Formaldehyde → 1-hydroxymethyl-4-fluoro-2-[[(4-methoxy-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole

HRID 728635
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 728635
[F:1][C:2]1[C:10]2[N:9]=[C:8]([S:11]([CH2:13][C:14]3[CH:19]=[C:18]([O:20][CH3:21])[CH:17]=[CH:16][N:15]=3)=[O:12])[NH:7][C:6]=2[CH:5]=[CH:4][CH:3]=1.[CH3:22][OH:23].C=O>C(Cl)Cl>[OH:23][CH2:22][N:7]1[C:6]2[CH:5]=[CH:4][CH:3]=[C:2]([F:1])[C:10]=2[N:9]=[C:8]1[S:11]([CH2:13][C:14]1[CH:19]=[C:18]([O:20][CH3:21])[CH:17]=[CH:16][N:15]=1)=[O:12]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 712FormaldehydeHCID 887MethanolHCID 156624894-fluoro-2-[[(4-methoxy-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole

Produkt 1

HCID 156624921-hydroxymethyl-4-fluoro-2-[[(4-methoxy-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

4-Fluoro-2-[[(4-methoxy-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole (1.6 g, 5.2 mmol) was suspended in methylene chloride (50 ml). Methanol was added until a clear solution was obtained. The mixture was concentrated on a rotavapor under reduced pressure. The oily residue, which was not allowed to crystallize, was dissolved in methylene chloride (30 ml). A solution of formaldehyde (5 M, 10 ml, 50 mmol) was added and the mixture was stirred violently for four minutes. After separation the organic solution was dried (Na2SO4) and concentrated until 10 ml of the mixture was left. The flask was chilled for 15 minutes whereupon the formed precipitate was filtered off and washed with cold methylene chloride. In this way the title compound was obtained (1.1 g, 63%). NMR data is given below.

Aufarbeitung

  1. customwas obtained
  2. concentrationThe mixture was concentrated on a rotavapor under reduced pressure
  3. customto crystallize
  4. dissolutionwas dissolved in methylene chloride (30 ml)
  5. customAfter separation the organic solution
  6. dry with materialwas dried (Na2SO4)
  7. concentrationconcentrated until 10 ml of the mixture
  8. waitwas left
  9. temperatureThe flask was chilled for 15 minutes whereupon the formed precipitate
  10. filtrationwas filtered off
  11. washwashed with cold methylene chloride

Quellen und Nachweise

ORD-Eintrag
ord-320ae4aa01a14de1868eab9a2ae4d2f4
Quelldatensatz
uspto-grants-1991_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05049674

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