Potassium Acetate → HCID 20269414, compound

HRID 485765Notes

Reaction equation

HRID 485765 reaction equation
Cl[CH2:2][C:3]1[N:4]=[C:5]2[S:12][CH:11]=[N:10][N:6]2[C:7](=[O:9])[CH:8]=1.[C:13]([O-:16])(=[O:15])[CH3:14].[K+]>CN(C)C=O>[C:13]([O:16][CH2:2][C:3]1[N:4]=[C:5]2[S:12][CH:11]=[N:10][N:6]2[C:7](=[O:9])[CH:8]=1)(=[O:15])[CH3:14]

Participants

4

Reactant 2

HCID 517044Potassium AcetateHCID 71307877-(chloromethyl)-5H-[1,3,4]thiadiazolo[3,2-a]pyrimidin-5-one(SALTDATA: FREE)

Product 1

HCID 20269414HCID 20269414, compoundYield 86.8%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

7-chloromethyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidine-5-one (10 g), prepared according to Example 1, was dissolved in dimethylformamide (40 ml) and reacted with anhydrous potassium acetate (10 g) under stirring at room temperature for 20 hours. After dilution with ice water the precipitate was filtered and washed with water to give 7-acetoxymethyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidine-5-one (9.7 g) which was hydrolyzed by treatment with 37% HCl (50 ml) in dioxane (100 ml) under stirring at room temperature for 2 hours. The reaction mixture was diluted with acetone and the precipitate was filtered and then treated with aqueous Na2HPO4 : filtration and washings with water until neutral gave 7-hydroxymethyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidine-5-one (6.2 g) which was reacted with dicyclohexylcarbodiimide (14.4 g) in benzene (90 ml) and dimethylsulphoxide (25 ml) in the presence of trifluoroacetic acid (1 ml) and pyridine (1.71 ml) under stirring at room temperature for 20 hours. After treatment with oxalic acid bihydrate (3.1 g) at room temperature, the precipitate of dicyclohexylurea was filtered of and the organic solution was evaporated in vacuo to dryness: the residue was purified over a SiO2 column using chloroform: ethyl acetate=95:5 as eluent. The 7-formyl-5H-1,3,4-thiadiazolo[3,2-a]pyrimidine-5-one so obtained (2.5 g) was reacted with the ylide obtained by treatment of triphenylphosphonium-benzyl chloride (2.94 g) with 50% NaH (0.43 g), in dimethylsulphoxide (40 ml) at room temperature for 22 hours. After dilution with ice water the precipitate was filtered and washed with water: crystallization from CH2Cl2 -ethanol gave 2.1 g of 7-trans-(2-phenyl-ethenyl)-5H-1,3,4-thiadiazolo[3,2-a]pyrimidine-5-one, m.p. 216°-218° C.

Workup

  1. filtrationAfter dilution with ice water the precipitate was filtered
  2. washwashed with water

Sources & evidence

ORD record
ord-8044d053599f4a368127a4dd67d12258
Source dataset
uspto-grants-1985_08
Patent number
US04537962

Reaction notes

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