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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | 2-methyl-2H-1,2,3,4-tetrazol-5-amine | HCID 138677 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | 2-(1-Methoxycycloheptyl)-5-(trifluoromethyl)benzaldehyde | HCID 58968666 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | N-(2-(1-methoxycycloheptyl)-5-(trifluoromethyl)benzyl)-2-methyl-2H-tetrazol-5-amine | HCID 58968736 | 55.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07919506B2 |
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| 출처 데이터셋 | uspto-grants-2011_04 |
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| ORD ID | ord-8414bfe90faf4f0f9317391bee544676 |
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| 출처 메모 | uspto-grants-2011_04 |
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