참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cyanogen Bromide | HCID 10476 | — |
| 반응물 | 2-Naphthohydrazide | HCID 123485 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 5-(Naphthalen-2-yl)-1,3,4-oxadiazol-2-amine | HCID 18707476 | 20% |
반응 단계
To a stirred solution of naphthalene-2-carboxylic acid hydrazide (0.6 g, 3.22 mmol, prepared as described in example 1) in dioxane (20 ml) was added a solution of sodium hydrogen carbonate (0.27 g, 3.22 mmol) in water (15 ml) and the resulting mixture was stirred for 5 min. To the reaction mixture was added cyanogen bromide (0.35 g, 3.3 mmol) and the mixture was stirred for 3 h at room temperature. The precipitate was filtered off and washed with diethyl ether (2×15 ml) and dried in vacuo at 50° C. affording 0.4 g of crude product which was suspended in absolute ethanol (15 ml) and stirred at reflux temperature for 0.5 h. The cooled suspension was filtered and the filter cake was dried in vacuo at 50° C. affording 130 mg (20%) of the title compound as a solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05958957 |
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| 출처 데이터셋 | uspto-grants-1999_09 |
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| ORD ID | ord-74ce89f4603944c88def162dc4d10b8f |
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| 출처 메모 | uspto-grants-1999_09 |
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