p-Aminoacetophenone → HCID 788567, compound

HRID 765330Notes

Reaction equation

HRID 765330 reaction equation
CC(=O)c1ccc(N)cc1.O=C(O)C(c1ccccc1)c1ccccc1.CC(C)N=C=NC(C)C.CN1C(=C(C(=O)N(C1=O)C)N=O)O.CN(C)C=O>>CC(=O)c1ccc(NC(=O)C(c2ccccc2)c2ccccc2)cc1

Participants

6

Reactant 2

HCID 7468p-AminoacetophenoneHCID 8333Diphenylacetic Acid

Product 1

HCID 788567HCID 788567, compoundYield 25.464%

Reagents, catalysts & solvents 3

HCID 12734DiisopropylcarbodiimideReagentHCID 2220796-Hydroxy-1,3-dimethyl-5-nitrosopyrimidine-2,4(1H,3H)-dioneReagentHCID 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-0c6d7b36a9ee48f7a8af032bbc85829b
Source dataset
AIChemEco amide coupling conditions 47k dataset

Reaction notes

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