Réaction #352027

Équation de réaction

N-methyl-6-nitrospiro[2H-1-benzopyran-2,4'-tetrahydropyran]-4-carbothioamide

2-chloro-1-methylpyridinium iodide

cyanamide

sodium hydride

→

N-cyano-N'-methyl-6-nitrospiro[2H-1-benzopyran-2,4'-tetrahydropyran]-4-amidine

Rendement 6.8%

Solvants

tetrahydrofuran

triethylamine

Conditions de réaction

Traitement

1. 1
   Températurewas refluxed
2. 2
   Températurewith heating for 2 hours
3. 3
   Températurethe reaction mixture was refluxed
4. 4
   Températurewith heating for 2 hours
5. 5
   Extractionthe resultant mixture was extracted with methylene chloride
6. 6
   LavageAn organic layer was washed with water
7. 7
   Autredried
8. 8
   workup.DISTILLATIONthe solvent was distilled
9. 9
   AutreThe obtained residue was purified
10. 10
    Autrerecrystallized by a mixed solvent of ethyl acetate and hexane

Mode opératoire

A mixture of 200 mg of N-methyl-6-nitrospiro[2H-1-benzopyran-2,4'-tetrahydropyran]-4-carbothioamide, 192 mg of 2-chloro-1-methylpyridinium iodide, 209 μl of triethylamine and 5 ml of dried tetrahydrofuran was refluxed with heating for 2 hours and further cooled to room temperature. 42 mg of cyanamide and 30 mg of sodium hydride (60%) were added therein and the reaction mixture was refluxed with heating for 2 hours. Ice water was added therein and the resultant mixture was extracted with methylene chloride. An organic layer was washed with water and dried, and the solvent was distilled. The obtained residue was purified according to silica gel column chromatography (developing solution, CH2Cl2) and recrystallized by a mixed solvent of ethyl acetate and hexane to obtain 14 mg of N-cyano-N'-methyl-6-nitrospiro[2H-1-benzopyran-2,4'-tetrahydropyran]-4-amidine with a melting point of 293°-294° C.

Source