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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78621생성일: 2026년 10월 24일

Triethylamine → 4-(5-amino-6-(2-(6-aminopyridine-2-carbonyl)hydrazinecarbonyl)pyrazin-2-yl)-N,N-dimethylbenzamide

https://huagongshe.com/ko/reaction/78621

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물6-Aminopyridine-2-carboxylic acidHCID 351652—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물4-(5-amino-6-(hydrazinecarbonyl)pyrazin-2-yl)-N,N-dimethylbenzamideHCID 59471641—
용매DimethylformamideHCID 6228—
생성물4-(5-amino-6-(2-(6-aminopyridine-2-carbonyl)hydrazinecarbonyl)pyrazin-2-yl)-N,N-dimethylbenzamideHCID 59472227—

반응 단계

A solution of 4-[5-amino-6-(hydrazinecarbonyl)pyrazin-2-yl]-N,N-dimethyl-benzamide (100 mg, 0.3163 mmol) and 6-aminopyridine-2-carboxylic acid (43.69 mg, 0.3163 mmol) in DMF (1.000 mL) was treated with triethylamine (32.01 mg, 44.09 μL, 0.3163 mmol) then warmed slightly. The mixture was cooled to room temperature and then treated with (benzotriazol-1-yloxy-dimethylamino-methylene)-dimethyl-ammonium tetrafluoroborate (121.9 mg, 0.3796 mmol) and stirred at room temperature overnight. The mixture was poured dropwise onto water (5 ml) with rapid stirring, stirred at room temperature for 1 h then filtered to give a wet paste which was dried under high vacuum at 100° C. overnight. Used directly in the next step without purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841308B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-04f9d786475440d3a8e31f38bff41582
출처 메모uspto-grants-2014_09