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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

반응식

참여 물질

역할이름HCID투입량
반응물NitroethaneHCID 6587—
반응물Phenyl isocyanateHCID 7672—
반응물TriethylamineHCID 8471—
반응물tert-Butyl (6-ethynyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylcarbamateHCID 57691050—
용매BenzeneHCID 241—
생성물Tert-butyl (6-(3-methylisoxazol-5-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methylcarbamateHCID 57691036—

반응 조건

온도50 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524900B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-d952825d729b4d20be4a45b727aa6332
출처 메모uspto-grants-2013_09