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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2075080생성일: 2026년 10월 27일

Ethanol → N-(2-(1-methoxycycloheptyl)-5-(trifluoromethyl)benzyl)-2-methyl-2H-tetrazol-5-amine

https://huagongshe.com/reaction/2075080

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물2-methyl-2H-1,2,3,4-tetrazol-5-amineHCID 138677—
반응물Sodium borohydrideHCID 4311764—
반응물2-(1-Methoxycycloheptyl)-5-(trifluoromethyl)benzaldehydeHCID 58968666—
용매TolueneHCID 1140—
생성물N-(2-(1-methoxycycloheptyl)-5-(trifluoromethyl)benzyl)-2-methyl-2H-tetrazol-5-amineHCID 5896873655.1%

반응 단계

A mixture of 2-(1-methoxycycloheptyl)-5-(trifluoromethyl)benzaldehyde (118 mg, 0.393 mmol) and 2-methyl-2H-tetrazol-5-amine (148 mg, 1.49 mmol) in toluene (3 mL) was heated at reflux for 16 hours, after which solvent was removed to give a gummy solid. Ethanol (3 mL) and sodium borohydride (25 mg; 0.660 mmol) were added to the residue. The resulting mixture was stirred at room temperature for 16 hours. Solvent was evaporated under reduced pressure. The residue was taken up in ethyl acetate and washed twice with water and dried over sodium sulfate and concentrated under reduced pressure. The crude was purified over 4 g RediSep (eluted with 20-60% ethyl acetate in heptane) to give 83 mg (55% yield) of title compound. MS (ES+): Calc: 383.4, Found: 352.3 (M-OMe). 1H NMR (400 MHz, CDCl3) δ ppm 7.84 (s, 1H), 7.48 (dd, J=8.77 Hz, 1H), 7.42 (d, J=8.30 Hz, 1H), 4.92 (d, J=6.22 Hz, 2H), 4.75 (t, J=6.22 Hz, 1H), 4.16 (s, 3H), 3.03 (s, 3H), 2.26 (m, 2H), 2.07 (m, 2H), 1.88-1.77 (m, 2H), 1.75-1.65 (m, 2H), 1.64-1.52 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07919506B2
출처 데이터셋uspto-grants-2011_04
ORD IDord-8414bfe90faf4f0f9317391bee544676
출처 메모uspto-grants-2011_04