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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18747생성일: 2026년 10월 24일

3-Fluorobenzylamine → tert-butyl (3aR,7aS)-2-[(3-fluorophenyl)methylamino]-3a,4,5,6,7,7a-hexahydrobenzimidazole-1-carboxylate

https://huagongshe.com/ko/reaction/18747

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참여 물질

역할이름HCID투입량
반응물3-FluorobenzylamineHCID 66853—
반응물cis-3a,4,5,6,7,7a-Hexahydro-2-methylthio-benzimidazole-1-carboxylic Acid, Tert-Butyl EsterHCID 86596330—
용매DichloromethaneHCID 6344—
생성물tert-butyl (3aR,7aS)-2-[(3-fluorophenyl)methylamino]-3a,4,5,6,7,7a-hexahydrobenzimidazole-1-carboxylateHCID 6856916673.2%

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온도100 °C

반응 단계

A mixture of intermediate 76 (200 mg, 0.0.740 mmol), 3-fluorobenzylamine (0.5 mL, 4.4 mmol) is heated at 100° C. (reaction block) overnight. The reaction mixture is cooled to RT. The reaction mixture is diluted with dichloromethane, washed with 0.1N HCl, and brine. The solvent is evaporated, and the residue triturated with EtOAc, and the insoluble material filtered to give 188 mg of the product 191. 1H NMR (CDCl3) δ 8.56 (s, 1 H), 7.45-7.20 (m, 3 H), 7.20-6.95 (m, 2 H), 5.20-4.95 (m, 2 H), 4.35-4.10 (m, 2 H), 2.75-2.55 (m, 1 H), 2.20-2.05 (m, 1 H), 1.80-1.05 (m, 15 H); MS: m/z 348 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741493B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-0e53e646914745f6a1fccb3386846b2b
출처 메모uspto-grants-2010_06