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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1435490생성일: 2026년 10월 26일

N-{2-tert-Butyl-1-[(4,4-difluorocyclohexyl)methyl]-1H-benzimidazol-5-yl}acetamide → 2-tert-Butyl-1-[(4,4-difluorocyclohexyl)methyl]-1H-benzimidazol-5-amine

https://huagongshe.com/reaction/1435490

반응식

참여 물질

역할이름HCID투입량
반응물N-{2-tert-Butyl-1-[(4,4-difluorocyclohexyl)methyl]-1H-benzimidazol-5-yl}acetamideHCID 57723211—
용매Ethanol hydrochlorideHCID 21887872—
생성물2-tert-Butyl-1-[(4,4-difluorocyclohexyl)methyl]-1H-benzimidazol-5-amineHCID 57723213—

반응 조건

온도120 °C

반응 단계

N-{2-tert-Butyl-1-[(4,4-difluorocyclohexyl)methyl]-1H-benzimidazol-5-yl}acetamide (500 mg, 1.37 mmol) was dissolved in 10 mL of 2 M HCl-EtOH (1:1). The solution was divided into two sealed tubes (5 mL/tube). Each tube was heated at 120° C. in a Personal Chemistry microwaves instrument for 1 h. The fractions were pooled and the solvent was evaporated. The residue was diluted with 2 M NaOH and extracted (3×) with EtOAc. The organic phase was washed with saturated aqueous NaCl solution and dried over anhydrous Na2SO4. The solvent was evaporated. Yield: 440 mg (99%); 1H NMR (400 MHz, CDCl3) δ 1.40-1.52 (m, 2 H), 1.52-1.54 (m, 9 H), 1.56-1.66 (m, 4 H), 1.68-1.75 (m, 2 H), 2.07-2.17 (m, 3 H), 4.14 (d, J=7.62 Hz, 2 H), 6.65 (dd, J=8.50, 2.25 Hz, 1 H), 7.04-7.09 (m, 2 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07615642B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-b7684c6d45964afb842312730427c1cd
출처 메모uspto-grants-2009_11