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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2053526생성일: 2026년 10월 25일

4-Fluorobenzylamine → tert-butyl (4S,5R)-2-[(4-fluorophenyl)methylamino]-4,5-diphenyl-4,5-dihydroimidazole-1-carboxylate

https://huagongshe.com/reaction/2053526

반응식

참여 물질

역할이름HCID투입량
반응물4-FluorobenzylamineHCID 67326—
반응물cis-4,5-Diphenyl-2-methylthio-4,5-dihydro-imidazole-1-carboxylic Acid, Tert-Butyl EsterHCID 86596320—
용매MethanolHCID 887—
생성물tert-butyl (4S,5R)-2-[(4-fluorophenyl)methylamino]-4,5-diphenyl-4,5-dihydroimidazole-1-carboxylateHCID 6856868041.6%

반응 조건

온도100 °C

반응 단계

A mixture of intermediate 59 (1.0 g, 0.0027 mol), 4-fluorobenzylamine (0.372 mL, 0.00321 mol) and MeOH (0.4 mL) is heated at 100° C. for 2 days. The reaction mixture is cooled to RT, and partitioned between dichloromethane and water. The organic solution is separated, dried (MgSO4), and concentrated in vacuo. The residue is purified by chromatography on silica gel; gradient elution with heptane:EtOAc (80:20-40:60) gives 0.50 g of the product 85. 1H NMR (CDCl3) δ 7.60-7.35 (m, 3H), 7.15-6.90 (m, 10H), 6.85-6.70 (m, 2H), 5.50-5.30 (m, 2H), 5.75-5.55 (m, 2H), 1.12 (s, 9H); MS: m/z 446 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07326792B2
출처 데이터셋uspto-grants-2008_02
ORD IDord-c8791c0e2c9448708eaf47ed6d2181c5
출처 메모uspto-grants-2008_02