Reaction #2358551

ord-3b8f9ee181bd412aaeb0eee78b901aca

Reaction equation

Cl
HCl
O=C(Cl)OCc1ccccc1
Cbz-Cl
CCOCOc1cc(OCc2ccccc2)c(-c2n[nH]c(=O)n2-c2ccc3c(ccn3C)c2)cc1C(C)C
3-(2-(benzyloxy)-4-(ethoxymethoxy)-5-isopropylphenyl)-4-(1-methyl-1H-indol-5-yl)-1H-1,2,4-triazol-5(4H)-one
CCN(C(C)C)C(C)C
DIPEA
CCOCOc1cc(OCc2ccccc2)c(-c2nn(C(=O)OCc3ccccc3)c(=O)n2-c2ccc3c(ccn3C)c2)cc1C(C)C
benzyl 3-(2-(benzyloxy)-4-(ethoxymethoxy)-5-isopropylphenyl)-4-(1-methyl-1H-indol-5-yl)-5-oxo-4,5-dihydro-1H-1,2,4-triazole-1-carboxylate

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    WashWashed with water
  2. 2
    Extractionextracted with dichloromethane and solvent
  3. 3
    Otherwas removed
  4. 4
    OtherThe crude reaction mixture
  5. 5
    Otherwas carried over to the next reaction without further purification
  6. 6
    Temperatureheated it up to 65° C

Procedure

Cbz-Cl was added to the solution of 3-(2-(benzyloxy)-4-(ethoxymethoxy)-5-isopropylphenyl)-4-(1-methyl-1H-indol-5-yl)-1H-1,2,4-triazol-5(4H)-one and DIPEA in dichloromethane and reaction solution was stirred for 2 h at room temperature. Washed with water and extracted with dichloromethane and solvent was removed. The crude reaction mixture was carried over to the next reaction without further purification. The reaction mixture was diluted by methanol and treated with concentrated HCl and heated it up to 65° C. Column chromatogram produced the desired benzyl 3-(2-(benzyloxy)-4-(ethoxymethoxy)-5-isopropylphenyl)-4-(1-methyl-1H-indol-5-yl)-5-oxo-4,5-dihydro-1H-1,2,4-triazole-1-carboxylate.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09120745B2uspto-grants-2015_09