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Methyl iodide → 2-Methylsulfanyl-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazole-4-carboxylic acid ethyl ester

HRID 1508094
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1508094
[CH2:1]([O:3][C:4]([C:6]1[NH:7][C:8]([SH:11])=[N:9][CH:10]=1)=[O:5])[CH3:2].[CH2:12](N(CC)CC)C.IC.[CH3:21][Si:22]([CH2:25][CH2:26][O:27][CH2:28]Cl)([CH3:24])[CH3:23]>C(Cl)Cl>[CH2:1]([O:3][C:4]([C:6]1[N:7]([CH2:28][O:27][CH2:26][CH2:25][Si:22]([CH3:24])([CH3:23])[CH3:21])[C:8]([S:11][CH3:12])=[N:9][CH:10]=1)=[O:5])[CH3:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 6328Methyl iodideHCID 8471Triethylamine3×HCID 27242712-Chloromethyl 2-(trimethylsilyl)ethyl ether2×HCID 178469868ethyl 2-sulfanyl-1H-imidazole-5-carboxylate

Produkt 1

HCID 589945432-Methylsulfanyl-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazole-4-carboxylic acid ethyl esterAusbeute 55 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

To a solution of 2-mercapto-3H-imidazole-4-carboxylic acid ethyl ester (1.0 g, 5.8 mmol) in 15 mL of DCM was added triethylamine (NEt3) (1.0 mL, 7.2 mmol) and iodomethane (0.4 mL, 6.4 mmol) and the mixture stirred for 3 h at RT. The mixture was cooled in an ice bath, NEt3 (1.0 mL, 7.2 mmol) and SEM-Cl (1.2 mL, 6.4 mmol) was added, the mixture stirred for 3 hours at RT and then an additional portion of NEt3 (0.5 mL, 3.6 mmol) and SEM-Cl (0.6 mL, 3.2 mmol) was added and the mixture stirred for 8 h at RT. The mixture was diluted with 50 mL of DCM and washed with NaHCO3 (2×60 mL) and brine (60 mL) and dried over Na2SO4. Flash chromatography of the residue on Si gel with 30% EtOAc/hexanes gave the title compound as a colorless oil (1.0 g, 55%). Mass spectrum (ESI, m/z): Calcd. for C13H24N2O3SSi, 317.1 (M+H). found 316.7.

Aufarbeitung

  1. temperatureThe mixture was cooled in an ice bath
  2. stirringthe mixture stirred for 3 hours at RT
  3. stirringthe mixture stirred for 8 h at RT
  4. washwashed with NaHCO3 (2×60 mL) and brine (60 mL)
  5. dry with materialdried over Na2SO4

Quellen und Nachweise

ORD-Eintrag
ord-247abd97e3b24cd59463b525b2547b76
Quelldatensatz
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09221797B2

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