Sodium Chloride → HCID 23086906, compound

HRID 900833Notes

Reaction equation

HRID 900833 reaction equation
CS([C:5]1[N:9]=[C:8]([C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([F:16])[CH:11]=2)[S:7][N:6]=1)(=O)=O.[CH2:17]([OH:21])[C:18]#[C:19][CH3:20].[H-].[Na+].[Cl-].[Na+]>CN(C)C=O>[F:16][C:12]1[CH:11]=[C:10]([C:8]2[S:7][N:6]=[C:5]([O:21][CH2:17][C:18]#[C:19][CH3:20])[N:9]=2)[CH:15]=[CH:14][CH:13]=1

Participants

6

Reactant 4

HCID 5234Sodium ChlorideHCID 129912-Butyn-1-olHCID 24758Sodium hydrideHCID 23086897HCID 23086897, compound

Product 1

HCID 23086906HCID 23086906, compoundYield 85.9%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

In 3 ml of N,N-dimethylformamide, 350 mg of 3-methylsulfonyl-5-(3-fluorophenyl)-1,2,4-thiadiazole and 105 mg of 2-butyne-1-ol were dissolved, to the resulting solution was added 65 mg of sodium hydride (60% oily) with ice-cooling, and the mixture was stirred for 10 minutes, and further stirred at room temperature for 4 hours. Then, the reaction mixture was poured into an aqueous saturated sodium chloride solution, and the mixture was extracted with t-butyl methyl ether. The residue obtained by concentration of the organic layer was subjected to silica gel column chromatography to obtain 289 mg of 5-(3-fluorophenyl)-3-(2-butynyloxy)-1,2,4-thiadiazole (the compound (6) of the present invention).

Workup

  1. temperaturecooling
  2. stirringfurther stirred at room temperature for 4 hours
  3. extractionthe mixture was extracted with t-butyl methyl ether
  4. customThe residue obtained by concentration of the organic layer

Sources & evidence

ORD record
ord-7206decd61cc4bdba8e09ee2a0875899
Source dataset
uspto-grants-2008_04
Patent number
US07361675B2

Reaction notes

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