Reaction #838970
ord-563d622c4a66430692f30ac729ed52e5
Reaction equation
Cc1ccc(CC(=O)O)cc1
NCc1ccc(Cl)cc1
→
Cc1ccc(CC(=O)NCc2ccc
Yield 40.4%
Reactants
Conditions
Temperature
25°CELSIUS
Workup
- 1workup.ADDITION150 uL of MeCN/H2O (1:1) mixed solvent was dispensed separately into each plate using the 96-tip head of the Tecan Evo-200.
- 2workup.ADDITION150 uL of internal standard solution was dispensed separately into each plate using the 96-tip head of the Tecan Evo-200.
- 3workup.ALIQUOT10 uL aliquot taken from reaction vials, and added to pre-filled wells in the transfer plate.
- 4workup.ADDITION380 uL MeCN solvent were added to the transfer plate
- 5workup.ALIQUOT20 uL taken from transfer plate to filter plate 1 for LCMS analysis
- 6workup.ADDITION180 uL MeCN added to filter plate 1 for LCMS analysis
- 7workup.ALIQUOT10 uL taken from transfer plate to filter plate 2 for TOF-DESI analysis
- 8workup.ADDITION190 uL MeCN added to filter plate 2 for TOF-DESI analysis
- 9Otherthe 96-well filter plates were centrifuged for 2.5 min at 3000 RPM
Source
AIChemEco amide coupling conditions 47k dataset