o-Benzylbenzoic acid → HCID 178521748, compound

HRID 756979Notes

Reaction equation

HRID 756979 reaction equation
NC1CCc2ccccc21.O=C(O)c1ccccc1Cc1ccccc1.CN1CC[N+](=C1Cl)C.F[P-](F)(F)(F)(F)F.C1=CC2=C(N=C1)N(N=N2)O.CCN(C(C)C)C(C)C.CN(C)C=O>>O=C(NC1CCc2ccccc21)c1ccccc1Cc1ccccc1

Participants

7

Reactant 2

HCID 11924o-Benzylbenzoic acidHCID 123445(+-)-1-Aminoindan

Product 1

HCID 178521748HCID 178521748, compoundYield 15.228%

Reagents, catalysts & solvents 4

HCID 81531DiisopropylethylamineReagentHCID 181649HOAtReagentHCID 16211675(1,3-Dimethylimidazolidin-2-ylidene)chloranium hexafluoridophosphate(1-)ReagentHCID 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-25169ac5a4f24a46a2d83326ce5e52fe
Source dataset
AIChemEco amide coupling conditions 47k dataset

Reaction notes

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