Triethylamine → HCID 22504425, compound

HRID 1432277Notes

Reaction equation

HRID 1432277 reaction equation
[CH3:1][Si:2]([C:5]#[CH:6])([CH3:4])[CH3:3].[C:7]1([S:13]([NH:16][C:17]2[C:22](I)=[CH:21][C:20]([S:24][CH3:25])=[CH:19][N:18]=2)(=[O:15])=[O:14])[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.C(N(CC)CC)C.O1CCOCC1>C(OCC)(=O)C.O>[C:7]1([S:13]([N:16]2[C:17]3=[N:18][CH:19]=[C:20]([S:24][CH3:25])[CH:21]=[C:22]3[CH:6]=[C:5]2[Si:2]([CH3:4])([CH3:3])[CH3:1])(=[O:14])=[O:15])[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1

Participants

7

Reactant 4

HCID 8471TriethylamineHCID 312751,4-DioxaneHCID 66111TrimethylsilylacetyleneHCID 154868512-Benzenesulfonylamino-3-iodo-5-methylthiopyridine

Product 1

HCID 22504425HCID 22504425, compoundYield 80.3%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 8857Ethyl AcetateSolvent

Procedure

A mixture of trimethylsilylacetylene (0.41 g), 2-benzenesulfonylamino-3-iodo-5-methylthiopyridine (0.82 g), triethylamine (0.42 g), cuprous iodide (30 mg), dichlorobis (triphenylphosphine) palladium. (75 mg) and dioxane (2 ml) was stirred at 70° C. for 16 hours under nitrogen atmosphere. To the reaction solution were then added water and ethyl acetate. The insolubles were filtered off. To the filtrate was added a saturated aqueous sodium hydrogencarbonate solution, and the mixture was extracted with ethyl acetate, dried over anhydrous sodium sulfate, filtered and concentrated. The resulting residue was subjected to silica gel column chromatography (hexane:ethyl acetate=10:1) to obtain 0.61 g of the desired product.

Workup

  1. filtrationThe insolubles were filtered off
  2. additionTo the filtrate was added a saturated aqueous sodium hydrogencarbonate solution
  3. extractionthe mixture was extracted with ethyl acetate
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-cab9b7a2e3d244dfa8791ebcb339b5d6
Source dataset
uspto-grants-2009_11
Patent number
US07612070B2

Reaction notes

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