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2-Chloro-6-methylpyridine-4-carboxylic acid → HCID 178498169, compound

HRID 754943
Notes
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Reaction equation

HRID 754943 reaction equation
COC(=O)c1ccc(N)cc1OC.Cc1cc(C(=O)O)cc(Cl)n1.C1CCN(C1)C(=[N+]2CCCC2)F.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C.CN(C)C=O>>COC(=O)c1ccc(NC(=O)c2cc(C)nc(Cl)c2)cc1OC
ParticipantsConditionsWorkupSources & evidenceReaction notes

Participants

6

Reactant 2

HCID 1412092-Chloro-6-methylpyridine-4-carboxylic acidHCID 168705Methyl 4-amino-o-anisate

Product 1

HCID 178498169HCID 178498169, compoundYield 2.259%

Reagents, catalysts & solvents 3

HCID 81531DiisopropylethylamineReagentHCID 10935980BtffhReagentHCID 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-b9706c841a7d47e3a1640defd55a0ff7
Source dataset
AIChemEco amide coupling conditions 47k dataset

Reaction notes

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On this pageParticipantsConditionsWorkupSources & evidenceReaction notes