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HRID 1060426생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1060426

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 번호US06521666B1
출처 데이터셋uspto-grants-2003_02
ORD IDord-358f1c936d364d5e8ed4ccaf1863b67c
출처 메모uspto-grants-2003_02