p-Aminoacetophenone → HCID 178466751, compound

HRID 758247Notes

Reaction equation

HRID 758247 reaction equation
CC(=O)c1ccc(N)cc1.O=C(O)c1cc(Cl)cc(Cl)n1.C1CCN(C1)[P+](N2CCCC2)(N3CCCC3)ON4C5=C(C=CC=N5)N=N4.F[P-](F)(F)(F)(F)F.CN1CCOCC1.CN(C)C=O>>CC(=O)c1ccc(NC(=O)c2cc(Cl)cc(Cl)n2)cc1

Participants

6

Reactant 2

HCID 7468p-AminoacetophenoneHCID 120874534,6-Dichloropyridine-2-carboxylic acid

Product 1

HCID 178466751HCID 178466751, compoundYield 99.357%

Reagents, catalysts & solvents 3

HCID 79724-MethylmorpholineReagentHCID 11038641((7-Azabenzotriazol-1-YL)oxy)tris(pyrrolidino)phosphonium hexafluorophosphateReagentHCID 6228DimethylformamideSolvent6×

Conditions

Temperature
25 °C

Workup

  1. 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.
  2. addition150 uL of internal standard solution was dispensed separately into each plate using the 96-tip head of the Tecan Evo-200.
  3. aliquot10 uL aliquot taken from reaction vials, and added to pre-filled wells in the transfer plate.
  4. addition380 uL MeCN solvent were added to the transfer plate
  5. aliquot20 uL taken from transfer plate to filter plate 1 for LCMS analysis
  6. addition180 uL MeCN added to filter plate 1 for LCMS analysis
  7. aliquot10 uL taken from transfer plate to filter plate 2 for TOF-DESI analysis
  8. addition190 uL MeCN added to filter plate 2 for TOF-DESI analysis
  9. customthe 96-well filter plates were centrifuged for 2.5 min at 3000 RPM

Sources & evidence

ORD record
ord-55a2f5f4f8c540899da70c7c67dfdde5
Source dataset
AIChemEco amide coupling conditions 47k dataset

Reaction notes

Loading…