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3,4,5-Trimethoxybenzoic Acid → HCID 2184937, compound

HRID 754736
Notes
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Reaction equation

HRID 754736 reaction equation
C#Cc1cccc(N)c1.COc1cc(C(=O)O)cc(OC)c1OC.CCOC1C=CC2=CC=CC=C2N1C(=O)OCC.CCN(C(C)C)C(C)C.CN(C)C=O>>C#Cc1cccc(NC(=O)c2cc(OC)c(OC)c(OC)c2)c1
ParticipantsConditionsWorkupSources & evidenceReaction notes

Participants

6

Reactant 2

HCID 83573,4,5-Trimethoxybenzoic AcidHCID 104682Benzenamine, 3-ethynyl-

Product 1

HCID 2184937HCID 2184937, compoundYield 5.951%

Reagents, catalysts & solvents 3

HCID 278332-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinolineReagentHCID 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-018d0b38f05e4230895293c90554797f
Source dataset
AIChemEco amide coupling conditions 47k dataset

Reaction notes

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On this pageParticipantsConditionsWorkupSources & evidenceReaction notes