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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49982생성일: 2026년 10월 23일

Water → (7aS,6S)-2-(3,5-dichloro-phenyl)-6-(4-bromophenoxy)-tetrahydro-pyrrolo[1,2-c]imidazole-1,3-dione

https://huagongshe.com/ko/reaction/49982

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물3,5-Dichlorophenyl isocyanateHCID 94460—
반응물Methyl (2S,4S)-4-(4-bromophenoxy)-2-pyrrolidinecarboxylateHCID 26192761—
용매DimethylformamideHCID 6228—
생성물(7aS,6S)-2-(3,5-dichloro-phenyl)-6-(4-bromophenoxy)-tetrahydro-pyrrolo[1,2-c]imidazole-1,3-dioneHCID 9804074—

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온도20 °C

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The compound of formula (II), wherein R11 is 4-bromo, m is 0, W=O, and the bonds depicted as wavy bonds define the 7aS,6S stereoisomer, was prepared as follows. To a solution of cis-4-(4-bromo-phenoxy)-L-proline methyl ester (0.2 g) (0.66 mmol) (Preparation 4) and K2CO3 (0.09 g) (1 eq.) in 10 mL of DMF at 0° C. was added 3,5-dichlorophenyl isocyanate (0.12 g) (1 eq.). The reaction mixture was allowed to warm to 20° C. and was stirred overnight. After adding water, the mixture was extracted with EtOAc. The combined organic extracts were washed with water, dried over MgSO4, and evaporated under reduced pressure to afford after SiO2 chromatography (eluent: DCM), the above-titled compound (60 mg). Mp=116° C. NMR (DMSO, 200 MHz): 7.75 (1H, m), 7.5-7.4 (4H, d+d), 6.85 (2H, d), 5.1 (1H, m), 4.6 (1H, dd), 3.95 (1H, dd), 3.35 (1H, dd), 2.7-2.5 (1H, m), 2.25 (1H, bd).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710064B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-d08659727858425597f2d5fe8444c906
출처 메모uspto-grants-2004_03