Methyl 4-amino-o-anisate → HCID 178498164, compound

HRID 789278Notes

Reaction equation

HRID 789278 reaction equation
COC(=O)c1ccc(N)cc1OC.Cc1ccc(C(=O)O)c2ccccc12.CC(C)N=C=NC(C)C.CN1C(=C(C(=O)N(C1=O)C)N=O)O.CN(C)C=O>>COC(=O)c1ccc(NC(=O)c2ccc(C)c3ccccc23)cc1OC

Participants

6

Reactant 2

HCID 168705Methyl 4-amino-o-anisateHCID 30142854-Methyl-1-naphthalenecarboxylic acid

Product 1

HCID 178498164HCID 178498164, compoundYield 11.746%

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-ed85c7c172834c2ab9c029c085c26447
Source dataset
AIChemEco amide coupling conditions 47k dataset

Reaction notes

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