反応 #44879

反応方程式

1-isopropyl-1,3-dihydro-2H-benzimidazol-2-one

chloroformic acid 4-nitrophenyl ester

1-{[4-(aminomethyl)piperidin-1-yl]methyl}cyclobutanecarboxylic acid 4-methylbenzene sulfonate

1-{[4-(aminomethyl)piperidin-1-yl]methyl}cyclobutanecarboxylic acid 4-methylbenzenesulfonate

Et3N

Et3N

→

titled compound

1-{[4-({[(3-Isopropyl-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)carbonyl]amino}methyl)piperidin-1-yl]methyl}cyclobutanecarboxylic acid

溶媒

CH2Cl2

CH2Cl2

反応条件

後処理

1. 1
   workup.STIRRINGAfter stirring for 10 min
2. 2
   workup.STIRRINGthe resulting mixture was stirred at room temperature for 2 hr
3. 3
   洗浄This mixture was washed with 0.5 N HCl aq (10 mL) and saturated NaHCO3 aq (10 mL)
4. 4
   濃縮the organic layer was concentrated
5. 5
   workup.ADDITIONTo the residue, saturated NaHCO3 aq (15 mL) and heptane (15 mL) was added at room temperature
6. 6
   workup.STIRRINGit was stirred for 6 hrs at that temperature
7. 7
   ろ過this mixture was filtered
8. 8
   洗浄The obtained solid was washed with H2O and heptane
9. 9
   その他After drying
10. 10
    その他crude material was obtained (1.0 g, 82%) as white solid
11. 11
    その他This crude material (4.0 g) was purified by recrystallization from toluene (36 mL)

実験手順

A mixture of 1-isopropyl-1,3-dihydro-2H-benzimidazol-2-one (486 mg, 2.8 mmol) and chloroformic acid 4-nitrophenyl ester (556 mg, 2.8 mmol) in CH2Cl2 (10 mL) was stirred at room temperature for 5 min. To this mixture, Et3N (0.84 mL, 6.1 mmol) was added slowly and this mixture became a solution. This solution was added to a mixture of 1-{[4-(aminomethyl)piperidin-1-yl]methyl}cyclobutanecarboxylic acid 4-methylbenzene sulfonate (1.1 g, 2.8 mmol, Step 7) in CH2Cl2 (5 mL) at room temperature. After stirring for 10 min, Et3N (0.38 mL, 2.8 mmol) was added and the resulting mixture was stirred at room temperature for 2 hr. This mixture was washed with 0.5 N HCl aq (10 mL) and saturated NaHCO3 aq (10 mL) then the organic layer was concentrated. To the residue, saturated NaHCO3 aq (15 mL) and heptane (15 mL) was added at room temperature and it was stirred for 6 hrs at that temperature. Solid was observed and this mixture was filtered. The obtained solid was washed with H2O and heptane. After drying, crude material was obtained (1.0 g, 82%) as white solid. This crude material (4.0 g) was purified by recrystallization from toluene (36 mL) to give 2.6 g of the titled compound (66%) as white solid.

出典