HCID 66849998, compound → HCID 66849895, compound

HRID 1175704Notes

Reaction equation

HRID 1175704 reaction equation
[CH3:1][O:2][C:3](=[O:36])[CH:4]([NH:28][C:29]([O:31][C:32]([CH3:35])([CH3:34])[CH3:33])=[O:30])[CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][CH2:14][CH2:15][CH2:16][NH:17]C(OCC2C=CC=CC=2)=O)=[CH:9][CH:8]=1>CO.[Pd]>[CH3:1][O:2][C:3](=[O:36])[CH:4]([NH:28][C:29]([O:31][C:32]([CH3:34])([CH3:33])[CH3:35])=[O:30])[CH2:5][O:6][C:7]1[CH:8]=[CH:9][C:10]([CH2:13][CH2:14][CH2:15][CH2:16][NH2:17])=[CH:11][CH:12]=1

Participants

4

Reactant 1

HCID 66849998HCID 66849998, compound

Product 1

HCID 66849895HCID 66849895, compoundYield 99.9%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 887MethanolSolvent

Procedure

Compound 12 (505 mg, 1.00 mmol) was dissolved in methanol (20 mL) and 10% palladium on carbon (100 mg) was added. The flask was evacuated, filled with hydrogen gas under balloon pressure and stirred overnight. Filtration through celite to remove the catalyst followed by removal of the solvent under reduced pressure provided compound 13 (366 mg, 98%). 1H NMR (300 MHz, CDCl3) δ 7.08 (d, 2H), 6.80 (d, 2H), 5.51 (d, 1H), 4.66 (m, 1H), 4.38 (m, 1H), 4.17 (m, 1H), 3.78 (s, 3H), 2.73 (m, 2H), 2.58 (m, 2H), 1.90 (br s, 2H), 1.62 (m, 2H), 1.50 (m, 2H), 1.48 (s, 9H).

Workup

  1. customThe flask was evacuated
  2. additionfilled with hydrogen gas under balloon pressure
  3. filtrationFiltration through celite
  4. customto remove the catalyst
  5. customfollowed by removal of the solvent under reduced pressure

Sources & evidence

ORD record
ord-1189f018e7ac47c3a0299a93a649c5f8
Source dataset
uspto-grants-2010_11
Patent number
US07842697B2

Reaction notes

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