참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Nicotinamidine hydrochloride | HCID 202042 | — |
| 반응물 | Sodium hydroxide ethanol | HCID 23692425 | — |
| 반응물 | N'-benzyl-3-(4-(trifluoromethoxy)phenyl)-1,2,4-oxadiazole-5-carbohydrazide | HCID 86711886 | — |
| 생성물 | HCID 178506365 | HCID 178506365 | 5.7% |
반응 단계
A mixture of N′-benzyl-3-(4-(trifluoromethoxy)phenyl)-1,2,4-oxadiazole-5-carbohydrazide (40 mg, 0.11 mmol) and nicotinimidamide hydrochloride (33 mg, 0.21 mmol) in 2N NaOH ethanol solution (1.1 mL, 0.21 mmol) was heated to 65° C. for 30 min. The mixture was cooled to RT and concentrated under reduced pressure. The crude mixture was taken up in NMP (0.5 mL) and heated to 140° C. for 2 h. The mixture was cooled to RT and partitioned between H2O (0.5 mL) and EtOAc (0.5 mL). The aqueous layer was extracted with EtOAc (3×0.5 mL). The combined organic layers were washed with H2O (3×0.5 mL) and brine (0.5 mL), dried (Na2SO4), filtered and concentrated under reduced pressure. The crude oil was purified by reverse-phase HPLC to provide the TFA salt as a white solid (1.8 mg, 3%): 1H NMR (600 MHz, CDCl3) δ ppm 8.93 (s, 1H), 8.79 (d, J=4.8 Hz, 1H), 8.29 (d, J=8.1 Hz, 2H), 8.08 (d, J=8.0 Hz, 1H), 7.52 (app. dd, J=7.5 Hz, 5.5 Hz, 1H), 7.37-7.30 (m, 5H), 7.20 (d, J=7.3 Hz, 2H), 5.62 (s, 2H); MS (ES+) C23H15F3N6O2 requires: 464. found: 465 [M+H]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09018380B2 |
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| 출처 데이터셋 | uspto-grants-2015_04 |
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| ORD ID | ord-e2d15a5b2e134a5dabf6cd855d003036 |
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| 출처 메모 | uspto-grants-2015_04 |
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