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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18749생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/18749

반응식

참여 물질

역할이름HCID투입량
반응물3,4-DifluorobenzylamineHCID 123572—
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-[(3,4-difluorophenyl)methylamino]-3a,4,5,6,7,7a-hexahydrobenzimidazole-1-carboxylateHCID 6856845199.8%

반응 조건

온도100 °C

반응 단계

A mixture of intermediate 76 (200 mg, 0.740 mmol), 3,4-difluorobenzylamine (0.5 mL, 4.2 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 270 mg of the product 195. 1H NMR (CDCl3) δ 8.60 (s, 1 H), 7.40-7.10 (m, 3 H), 5.15-4.90 (m, 2 H), 4.30-4.10 (m, 2 H), 2.70-2.55 (m, 1 H), 2.20-2.05 (m, 1 H), 1.85-1.10 (m, 15 H); MS: m/z 366 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741493B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-e28b7ea43af34b80a87b9ebc21e193e0
출처 메모uspto-grants-2010_06