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HRID 24654생성일: 2026년 10월 25일

Methyl isothiocyanate → N-[2-chloro-4-(3-methylthioureido)benzoyl]-4-(2-methoxyphenyl)-L-phenylalanine methyl ester

https://huagongshe.com/reaction/24654

반응식

참여 물질

역할이름HCID투입량
반응물Methyl isothiocyanateHCID 11167—
반응물DiisopropylethylamineHCID 81531—
반응물N-(4-amino-2-chlorobenzoyl)-4-(2-methoxyphenyl)-L-phenylalanine methyl esterHCID 54392214—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-[2-chloro-4-(3-methylthioureido)benzoyl]-4-(2-methoxyphenyl)-L-phenylalanine methyl esterHCID 54405488—

반응 조건

온도90 °C

반응 단계

Methylisothiocyanate (43 μL) was added to a solution of N-(4-amino-2-chlorobenzoyl)-4-(2-methoxyphenyl)-L-phenylalanine methyl ester (55.1 mg) in anhydrous DMF (1 mL) containing DIEA (22 μL) and DMAP (catalitic amount). The resulting mixture was then heated at 90° C. under N2 for 1 d. After cooling, the mixture was diluted with EtOAc, washed sequentially with 1N HCl, satd. NaHCO3 and water, dried (MgSO4) and evaporated. The residue was purified by preparative TLC (silica gel) using CH2Cl2/MeOH (15:1) as an eluent to give N-[2-chloro-4-(3-methylthioureido)benzoyl]-4-(2-methoxyphenyl)-L-phenylalanine methyl ester (22.7 mg). ESMS: m/z 512 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855843B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-258276ba663a44b99a5259d13e255860
출처 메모uspto-grants-2005_02