Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36209생성일: 2026년 10월 24일
5-n-Butyl-2,4-dihydro-4-[(2'-nitrobiphenyl-4-yl)methyl]-2-[2-(trifluoromethyl)phenyl]-3H-1,2,4-triazol-3-one → HCID 11754272, 화합물
https://huagongshe.com/ko/reaction/36209
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 5-n-Butyl-2,4-dihydro-4-[(2'-nitrobiphenyl-4-yl)methyl]-2-[2-(trifluoromethyl)phenyl]-3H-1,2,4-triazol-3-one | HCID 10480946 | — |
| 용매 | Hydrochloric Acid | HCID 313 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | HCID 11754272 | HCID 11754272 | 47% |
반응 단계
To a solution of 217 mg (0.438 mmole) of 5-n-butyl-2,4-dihydro-4-[(2'-nitrobiphenyl-4-yl)methyl]-2-[2-(trifluoromethyl)phenyl]-3H-1,2,4-triazol-3-one (from Step C) in 2.2 ml of THF stirred at 0° C. under N2 was added dropwise a solution of 692 mg (3.07 mmole) of stannous chloride dihydrate in 1.2 ml of concentrated hydrochloric acid. After 15 minutes, the ice bath was removed, and the mixture was allowed to warm to room temperature. After 2 hours at room temperature, by which time TLC (98:2 CH2Cl2 --MeOH) indicated complete disappearance of starting material, the reaction mixture was added to a mixture of 10.6 g of ice, 3 ml of 50% NaOH, and 6 ml of ether. The resulting mixture was stirred at 0° C. for about 1 hour and then extracted with 2×10 ml of ether and 1×10 ml of ethyl acetate. The combined organic extracts were washed with brine, dried over sodium sulfate, filtered, and concentrated. The crude product was flash chromatographed twice on silica gel (first elution with a gradient of 0.5-5% MeOH in CH2Cl2, second elution with 0.5% MeOH in CH2Cl2). Concentration of the product fractions afforded 95 mg (47%) of the title compound as a sticky foam; satisfactory purity by TLC (98:2 CH2Cl2 --MeOH) for use in the next step; mass spectrum (FAB) m/e 467 (M+1)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05411980 |
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| 출처 데이터셋 | uspto-grants-1995_05 |
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| ORD ID | ord-a5856dce1aab45f5bb41633e4481a463 |
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| 출처 메모 | uspto-grants-1995_05 |
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