Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40205생성일: 2026년 10월 23일
Nitroethane → Tert-butyl (6-(3-methylisoxazol-5-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylcarbamate
https://huagongshe.com/ko/reaction/40205
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Nitroethane | HCID 6587 | — |
| 반응물 | Phenyl isocyanate | HCID 7672 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | tert-Butyl (6-ethynyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylcarbamate | HCID 57691050 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | Tert-butyl (6-(3-methylisoxazol-5-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylcarbamate | HCID 57691036 | — |
반응 단계
To a solution of nitroethane (1.02 ml, 14.3 mmol) in benzene (50 mL) was added phenyl isocyanate (3.12 ml, 28.5 mmol). The mixture was stirred at 50° C. for twenty minutes followed by the addition of tert-butyl (6-ethynyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylcarbamate (3.00 g, 11.0 mmol) and triethylamine (0.0765 ml, 0.549 mmol). The mixture was stirred at 50° C. for six hours then at room temperature overnight. The mixture was cooled to room temperature, filtered and the resulting brown precipitate was washed with additional benzene. The filtrate was concentrated to yield the product as a black solid. MS m/z=331.1 [M+1]+. Calc'd for C15H18N6O3: 330.1.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08524900B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-d952825d729b4d20be4a45b727aa6332 |
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| 출처 메모 | uspto-grants-2013_09 |
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