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Potassium Acetate → HCID 59578523, compound

HRID 1627922
Notes
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Reaction equation

HRID 1627922 reaction equation
Br[C:2]1[C:11]2[C:6]3=[C:7]([CH2:12][CH2:13][O:14][C:5]3=[CH:4][CH:3]=1)[CH:8]=[CH:9][N:10]=2.[B:15]1(B2OC(C)(C)C(C)(C)O2)[O:19]C(C)(C)C(C)(C)[O:16]1.C([O-])(=O)C.[K+]>O1CCOCC1.C1CCC(P(C2CCCCC2)C2CCCCC2)CC1.C1CCC(P(C2CCCCC2)C2CCCCC2)CC1.[Pd]>[O:14]1[C:5]2[C:6]3[C:11]([C:2]([B:15]([OH:19])[OH:16])=[CH:3][CH:4]=2)=[N:10][CH:9]=[CH:8][C:7]=3[CH2:12][CH2:13]1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 517044Potassium AcetateHCID 2733548Bis(pinacolato)diboraneHCID 595785317-Bromo-2,3-dihydropyrano[4,3,2-de]quinoline

Product 1

HCID 59578523HCID 59578523, compoundYield 30.1%

Reagents, catalysts & solvents 2

HCID 2734559Bis(tricyclohexylphosphine) palladium(0)Catalyst
HCID 31275
1,4-Dioxane
Solvent

Conditions

Temperature
95 °C

Procedure

7-bromo-2.3-dihydropyrano[4.3.2-de]quinoline (0.170 g; 0.680 mmol), bis(pinacolato)diboron (0.207 g; 0.816 mmol), anhydrous potassium acetate (0.133 g; 1.36 mmol) and bis(tricyclohexylphosphine)palladium(0) (0.045 g; 0.068 mmol) in anhydrous 1.4-dioxane (3.1 mL) were mixed in a tube, purged with argon and sealed. After heating at 95° C. for 16 h, the mixture was cooled at room temperature, concentrated under reduced pressure and store at 3° C. for 21 h. The brown residue was dissolved in acetonitrile, filtered, and the dark brown solution was concentrated under reduced pressure. Purification by preparative HPLC (HPLC method 1) furnished 0.044 g (25%) of the title compound as an amorphous solid.

Workup

  1. custompurged with argon
  2. customsealed
  3. temperaturethe mixture was cooled at room temperature
  4. concentrationconcentrated under reduced pressure and store at 3° C. for 21 h
  5. dissolutionThe brown residue was dissolved in acetonitrile
  6. filtrationfiltered
  7. concentrationthe dark brown solution was concentrated under reduced pressure
  8. customPurification by preparative HPLC (HPLC method 1)

Sources & evidence

ORD record
ord-cdde1cd14ce040029e8179ce41f546e8
Source dataset
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08785638B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes