Reaktion #5988

ord-299b2716a8194ac09bde2f6df2151eb9

Reaktionsgleichung

COC(=O)Cl
methyl chloroformate
Cn1ccc2cc(Nc3ccncc3)ccc21
1-methyl-5-(4-pyridinylamino)-1H-indole
COC(=O)N(c1ccncc1)c1ccc2c(ccn2C)c1
solid
Ausbeute 98.4%
COC(=O)N(c1ccncc1)c1ccc2c(ccn2C)c1
N-(1-Methyl-1H-indol-5-yl)-N-(4-pyridinyl) carbamic acid methyl ester
Ausbeute 98.4%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwas washed with water and saturated sodium chloride
  2. 2
    Trocknendried (anhydrous magnesium sulfate)
  3. 3
    Filtrationfiltered
  4. 4
    Sonstigeevaporated to 4 g of a solid
  5. 5
    WaschenElution through silica with 50% ethyl acetate in dichloromethane via flash column chromatography

Vorschrift

A solution of methyl chloroformate (1.3 g) in 5 ml DCM was added to a solution of 1-methyl-5-(4-pyridinylamino)-1H-indole (2.5 g) in 120 ml DCM and 6 ml triethylamine (4.4 g). After stirring one hour at ambient temperature the reaction mixture was washed with water and saturated sodium chloride, dried (anhydrous magnesium sulfate), filtered and evaporated to 4 g of a solid. Elution through silica with 50% ethyl acetate in dichloromethane via flash column chromatography yielded 3.1 g of a solid. Recrystallization from methanol yielded 2.4 g of crystals, mp 157°-159° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05246947uspto-grants-1993_09