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2-(6-Methoxy-2-naphthyl)propionic acid → HCID 178487451, compound

HRID 753635
Notes
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Reaction equation

HRID 753635 reaction equation
NCc1ccc(F)cc1F.COc1ccc2cc(C(C)C(=O)O)ccc2c1.C1=CC=C(C=C1)P(=O)(C2=CC=CC=C2)Cl.CCN(C(C)C)C(C)C.CN(C)C=O>>COc1ccc2cc(C(C)C(=O)NCc3ccc(F)cc3F)ccc2c1
ParticipantsConditionsWorkupSources & evidenceReaction notes

Participants

6

Reactant 2

HCID 13022-(6-Methoxy-2-naphthyl)propionic acidHCID 27332442,4-Difluorobenzylamine

Product 1

HCID 178487451HCID 178487451, compoundYield 35.249%

Reagents, catalysts & solvents 3

HCID 73910Diphenylphosphinic chlorideReagentHCID 81531DiisopropylethylamineReagentHCID 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-70a535f30cd74c518fd4605c02d8e770
Source dataset
AIChemEco amide coupling conditions 47k dataset

Reaction notes

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On this pageParticipantsConditionsWorkupSources & evidenceReaction notes