Triethylamine → 1-((4-((((3-isopropyl-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)carbonyl)amino)methyl)piperidin-1-yl)methyl)cyclobutanecarboxylic acid

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.

1. stirringAfter stirring for 10 min
2. stirringthe resulting mixture was stirred at room temperature for 2 hr
3. washThis mixture was washed with 0.5 N HCl aq (10 mL) and saturated NaHCO3 aq (10 mL)
4. concentrationthe organic layer was concentrated
5. additionTo the residue, saturated NaHCO3 aq (15 mL) and heptane (15 mL) was added at room temperature
6. stirringit was stirred for 6 hrs at that temperature
7. filtrationthis mixture was filtered
8. washThe obtained solid was washed with H2O and heptane
9. customAfter drying
10. customcrude material was obtained (1.0 g, 82%) as white solid
11. customThis crude material (4.0 g) was purified by recrystallization from toluene (36 mL)

ORDレコード

ord-4c40678a5e8c473e978c0b8ce00bdfd3

出典データセット

uspto-grants-2010_06

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07737163B2