Reaction #1583837

ord-b78f19141324424e82594eb6322dc3f4

Reaction equation

COC(=O)NCc1cc(-c2cnn[nH]2)ccc1Cl
methyl N-[[2-chloro-5-(1H-1,2,3-triazol-5-yl)phenyl]methyl]carbamate
Clc1ccc(I)cc1
1-chloro-4-iodobenzene
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
COC(=O)NCc1cc(-c2cnn(-c3ccc(Cl)cc3)n2)ccc1Cl
methyl N-[[2-chloro-5-[2-(4-chlorophenyl)-2H-1,2,3-triazol-4-yl]phenyl]methyl]carbamate

Conditions

Temperature
110°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Concentrationconcentrated under reduced pressure
  2. 2
    Concentrationconcentrated onto silica gel (2 g)
  3. 3
    OtherThe silica gel mixture was purified by flash column chromatography

Procedure

A mixture of methyl N-[[2-chloro-5-(1H-1,2,3-triazol-5-yl)phenyl]methyl]carbamate (i.e. the product of Step E, Example 9) (0.53 g, 2.0 mmol), 1-chloro-4-iodobenzene (0.57 g, 2.4 mmol), iron(III) acetylacetonate (0.21 g, 0.6 mmol), copper(II) oxide (0.016 g, 0.2 mmol) and cesium carbonate (1.29 g, 4.0 mmol) in N,N-dimethylformamide (4 mL) was heated at 110° C. for 14 h and then concentrated under reduced pressure. The resulting residue was suspended in ethanol and then concentrated onto silica gel (2 g). The silica gel mixture was purified by flash column chromatography using a Supelco (division of Sigma-Aldrich Co., 595 North Harrison Road, Bellefonte, Pa. 16823, U.S.A.) tube prepacked with 10 g of silica gel (50 μm particle diameter, 70 Å pore size) and 3:1 hexanes-ethyl acetate as eluant to provide methyl N-[[2-chloro-5-[2-(4-chlorophenyl)-2H-1,2,3-triazol-4-yl]phenyl]methyl]carbamate, a compound of the present invention, as a beige solid (0.105 g)

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09198433B2uspto-grants-2015_12