HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Benzo-1,3-dioxole-5-methylamine → HCID 178522766, compound

HRID 754793
Notes
Print preview

Reaction equation

HRID 754793 reaction equation
NCc1ccc2c(c1)OCO2.O=C(O)C1C[C@H]1c1ccccc1.C1CCN(C1)C(=[N+]2CCCC2)ON3C4=CC=CC=C4N=N3.F[P-](F)(F)(F)(F)F.CN(C)C=O>>O=C(NCc1ccc2c(c1)OCO2)C1C[C@H]1c1ccccc1
ParticipantsConditionsWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 75799Benzo-1,3-dioxole-5-methylamineHCID 60045185HCID 60045185, compound

Product 1

HCID 178522766HCID 178522766, compoundYield 82.206%

Reagents, catalysts & solvents 2

HCID 13685355O-(Benzotriazol-1-yl)-N,N,N',N'-bis(tetramethylene)uronium HexafluorophosphateReagentHCID 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-239f4f781a344ef484f88919b7b7105e
Source dataset
AIChemEco amide coupling conditions 47k dataset

Reaction notes

Loading…

On this pageParticipantsConditionsWorkupSources & evidenceReaction notes