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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2204843생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2204843

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) weas 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 번호US09365557B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-bd6a801f443d4f73932e41f13583722b
출처 메모uspto-grants-2016_06