反応 #155372
ord-8f6931dbce994389892705f0d0639f67
反応方程式
1f
{4-[3-({2-[(4-Cyano-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}-phenyl-amino)-propionylamino]-butyl}-carbamic acid tert-butyl ester
ammonium carbonate
→
2-[(4-Carbamimidoyl-phenylamino)-methyl]-1-methyl-1H-benzoimidazole-5-carboxylic acid[2-(4-amino-butylcarbamoyl)-ethyl]-phenyl-amide
反応物
試薬
なし
反応条件
詳細条件
See reaction.notes.procedure_details.
後処理
- 1その他evaporated to dryness at 30° C
- 2workup.DISSOLUTIONThe remaining raw material was dissolved in 200 mL dry ethanol
- 3workup.STIRRINGthe mixture stirred at room temperature over night
- 4その他After evaporation of the solvent the remaining raw material
- 5その他was triturated with ca. 5 mL ethanol
- 6その他the undissolved material separated by filtration
- 7その他the solvent evaporated at 30° C
- 8workup.DISSOLUTIONThe product was then dissolved in 30 mL water
- 9workup.STIRRINGthe solution stirred with ca. 2 g charcoal
- 10ろ過filtered
- 11その他evaporated to dryness
実験手順
The product of 1f (4.81 mmol) was dissolved in a saturated solution of HCl in ethanol (250 mL), the mixture stirred at room temperature over night and then evaporated to dryness at 30° C. The remaining raw material was dissolved in 200 mL dry ethanol, then ammonium carbonate (48.1 mmol) was added and the mixture stirred at room temperature over night. After evaporation of the solvent the remaining raw material was triturated with ca. 5 mL ethanol, the undissolved material separated by filtration and the solvent evaporated at 30° C. The product was then dissolved in 30 mL water, the solution stirred with ca. 2 g charcoal, filtered and evaporated to dryness.