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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 970179생성일: 2026년 10월 24일

1-Hydroxybenzotriazole → Ethyl 3-[(3-oxo-6-pyridin-4-yl-2,3-dihydropyridazine-4-carbonyl)amino]propionate

https://huagongshe.com/ko/reaction/970179

반응식

참여 물질

역할이름HCID투입량
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물beta-Alanine, ethyl ester, hydrochlorideHCID 458475—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물3-Oxo-6-(pyridin-4-yl)-2,3-dihydropyridazine-4-carboxylic acidHCID 12790238—
용매DimethylformamideHCID 6228—
생성물Ethyl 3-[(3-oxo-6-pyridin-4-yl-2,3-dihydropyridazine-4-carbonyl)amino]propionateHCID 1031365732.9%

반응 조건

온도19 °C

반응 단계

0.733 g of 1-hydroxybenzotriazole, 0.833 g of β-alanine ethyl ester hydrochloride, 0.96 cm3 of N,N-diisopropylethylamine and 2.06 g of O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate were successively added to 0.94 g of 3-oxo-6-pyridin-4-yl-2,3-dihydropyridazine-4-carboxylic acid dissolved in 100 cm3 of N,N-dimethylformamide. The reaction medium was stirred for 12 hours at 19° C. The solvent was evaporated off under reduced pressure (2 kPa; 55° C.). The solid residue was triturated in 20 cm3 of dichloromethane, suction-filtered and oven-dried under reduced pressure (10 kPa; 20° C.). After purification by chromatography on silica gel (particle size 40-63 μm, under an argon pressure of 150 kPa) eluting with dichloromethane, 0.45 g of ethyl 3-[(3-oxo-6-pyridin-4-yl-2,3-dihydropyridazine-4-carbonyl)amino]propionate was obtained in the form of a white solid melting at 180° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07309701B2
출처 데이터셋uspto-grants-2007_12
ORD IDord-b4855d0d9f7847fab242bfcd36fd2200
출처 메모uspto-grants-2007_12