Triethylamine → HCID 57460530, compound

HRID 1673958Notes

Reaction equation

HRID 1673958 reaction equation
[CH2:1]([C:5]1[N:6]=[C:7]([CH3:36])[N:8]([C:27]2[CH:32]=[CH:31][CH:30]=[C:29]([CH:33]([OH:35])[CH3:34])[CH:28]=2)[C:9](=[O:26])[C:10]=1[CH2:11][C:12]1[CH:17]=[CH:16][C:15]([C:18]2[C:19]([C:24]#[N:25])=[CH:20][CH:21]=[CH:22][CH:23]=2)=[CH:14][CH:13]=1)[CH2:2][CH2:3][CH3:4].C(N(CC)CC)C.[C:44]([Si:48](Cl)([CH3:50])[CH3:49])([CH3:47])([CH3:46])[CH3:45].C(OCC)(=O)C>CN(C)C1C=CN=CC=1.CN(C)C=O.O>[CH2:1]([C:5]1[N:6]=[C:7]([CH3:36])[N:8]([C:27]2[CH:32]=[CH:31][CH:30]=[C:29]([CH:33]([O:35][Si:48]([C:44]([CH3:47])([CH3:46])[CH3:45])([CH3:50])[CH3:49])[CH3:34])[CH:28]=2)[C:9](=[O:26])[C:10]=1[CH2:11][C:12]1[CH:13]=[CH:14][C:15]([C:18]2[C:19]([C:24]#[N:25])=[CH:20][CH:21]=[CH:22][CH:23]=2)=[CH:16][CH:17]=1)[CH2:2][CH2:3][CH3:4]

Participants

8

Reactant 4

HCID 8471TriethylamineHCID 8857Ethyl AcetateHCID 28928tert-Butyldimethylsilyl chlorideHCID 57460529HCID 57460529, compound

Product 1

HCID 57460530HCID 57460530, compound

Reagents, catalysts & solvents 3

HCID 142844-(Dimethylamino)pyridineCatalystHCID 962WaterSolventHCID 6228DimethylformamideSolvent

Procedure

To a solution of 4′-({4-butyl-1-[3-(1-hydroxyethyl)phenyl]-2-methyl-6-oxo-1,6-dihydropyrimidin-5-yl}methyl)biphenyl-2-carbonitrile (1.86 g), triethylamine (1.1 mL) and 4-dimethylaminopyridine (0.15 g) in N,N-dimethylformamide (20 mL) was added tert-butyl(chloro)dimethylsilane (0.88 g), and the mixture was stirred for 15 hr. Ethyl acetate and water were added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated. The residue was purified by silica gel column chromatography to give the title compound as a pale-yellow viscous substance (1.98 g, 86%).

Workup

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe organic layer was washed with saturated brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customthe solvent was evaporated
  5. customThe residue was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-0ef4af1130614ac4893c351a754ecde8
Source dataset
uspto-grants-2011_08
Patent number
US07998968B2

Reaction notes

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