Potassium Carbonate → 8-methyl-3,4-dihydro-2H-[1,3]thiazino[3,2-a]benzimidazole

HRID 1926492ノート

反応式

HRID 1926492 の反応式
[SH:1][C:2]1[NH:3][C:4]2[CH:10]=[C:9]([CH3:11])[CH:8]=[CH:7][C:5]=2[N:6]=1.C(=O)([O-])[O-].[K+].[K+].I[CH2:19][CH2:20][CH2:21]I>CN(C)C=O>[CH3:11][C:9]1[CH:8]=[CH:7][C:5]2[N:6]3[CH2:21][CH2:20][CH2:19][S:1][C:2]3=[N:3][C:4]=2[CH:10]=1

参加物

5

反応物 3

HCID 11430Potassium CarbonateHCID 123141,3-DiiodopropaneHCID 178423448HCID 178423448、化合物

生成物 1

HCID 666281468-methyl-3,4-dihydro-2H-[1,3]thiazino[3,2-a]benzimidazole収率 25.3%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a flask were added 2 g 2-mercapto-5-methylbenzimidazole, 4.2 g potassium carbonate, 4.0 g 1,3-diiodopropane and 60 ml N,N-dimethylformamide. The mixture was heated to 50 C under nitrogen for 5 hours and then cooled to 22 C. The reaction was quenched with 100 ml water and the product was extracted twice with ethyl acetate and washed twice with water. Following removal of the solvent, the product was recrystallized by dissolving in a hot mixture of 50 ml hexane with 10 ml 2-propanol. After cooling to 5 C, the product was filtered, washed with hexane and dried giving 0.63 g of an off-white solid.

後処理

  1. temperatureThe mixture was heated to 50 C under nitrogen for 5 hours
  2. temperaturecooled to 22 C
  3. customThe reaction was quenched with 100 ml water
  4. extractionthe product was extracted twice with ethyl acetate
  5. washwashed twice with water
  6. customremoval of the solvent
  7. customthe product was recrystallized
  8. dissolutionby dissolving in a hot mixture of 50 ml hexane with 10 ml 2-propanol
  9. temperatureAfter cooling to 5 C
  10. filtrationthe product was filtered
  11. washwashed with hexane
  12. customdried

出典と根拠

ORDレコード
ord-82efc03176df4812bbd39c2761054352
出典データセット
uspto-grants-2012_05
特許番号
US08182718B2

反応ノート

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