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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 242770생성일: 2026년 10월 27일

4-Methylmorpholine → [(S)-1-(7-Methyl-1-phenyl-1H-benzoimidazol-2-yl)ethyl]carbamic acid benzyl ester

https://huagongshe.com/reaction/242770

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물N-carbobenzyloxyalanineHCID 736104—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물3-Methyl-N2-phenyl-1,2-benzenediamineHCID 68157147—
용매DichloromethaneHCID 6344—
생성물[(S)-1-(7-Methyl-1-phenyl-1H-benzoimidazol-2-yl)ethyl]carbamic acid benzyl esterHCID 6815751790.5%

반응 단계

To a solution of 3-methyl-N2-phenyl-benzene-1,2-diamine (852 mg, 4.3 mmol) in anhydrous DCM (20 mL) were added (S)-2-benzyloxycarbonylaminopropionic acid (1.44 g, 6.45 mmol), HOBt (639 mg, 4.73 mmol), 4-methylmorpholine (1.04 mL, 9.46 mmol) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (1.24 g, 6.45 mmol). The mixture was stirred at RT for 6.5 h and then partitioned between DCM (100 mL) and water. The organic layer was then washed with brine, dried (Na2SO4) and concentrated in vacuo. The resulting residue was dissolved in AcOH (10 mL) and heated to 65° C. for 18 h. After cooling to RT, volatiles were removed under reduced pressure and the residue diluted with EtOAc (100 mL). The organic layer was washed with a saturated solution of NaHCO3, followed by brine, then dried (Na2SO4) and concentrated in vacuo affording [(S)-1-(7-Methyl-1-phenyl-1H-benzoimidazol-2-yl)ethyl]carbamic acid benzyl ester as brown foam (1.5 g, 90%). LCMS: RT 3.07 min [M+H]+ 386.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653089B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-5d92de7fe1a84244b88539d299b4d77a
출처 메모uspto-grants-2014_02