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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18748생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/18748

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참여 물질

역할이름HCID투입량
반응물4-FluorobenzylamineHCID 67326—
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-[(4-fluorophenyl)methylamino]-3a,4,5,6,7,7a-hexahydrobenzimidazole-1-carboxylateHCID 6856943298.1%

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온도100 °C

반응 단계

A mixture of intermediate 76 (200 mg, 0.0.740 mmol), 4-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 252 mg of the product 193. 1H NMR (CDCl3) δ 8.55 (s, 1 H), 7.55-7.35 (m, 2 H), 7.10-7.00 (m, 2 H), 5.10-4.90 (m, 2 H), 4.30-4.10 (m, 2 H), 2.70-2.55 (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-55c3c36fc7e34f6d9b1a5a99f0ea5893
출처 메모uspto-grants-2010_06