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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1434709생성일: 2026년 10월 26일

4-Methylmorpholine → 2-[(2-bromo-pyridin-4-ylmethyl)-amino]-N-(2-methyl-2H-indazol-6-yl)-benzamide

https://huagongshe.com/reaction/1434709

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물2-Methyl-2H-indazol-6-amineHCID 590220—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물2-[(2-Bromo-pyridin-4-ylmethyl)-amino]benzoic AcidHCID 23118993—
용매DimethylformamideHCID 6228—
용매Sodium BicarbonateHCID 516892—
생성물2-[(2-bromo-pyridin-4-ylmethyl)-amino]-N-(2-methyl-2H-indazol-6-yl)-benzamideHCID 2311897296%

반응 단계

0.500 g (1.6 mmol) of 2-[(2-bromo-pyridin-4-ylmethyl)-amino]-benzoic acid, 0.471 g (3.2 mmol) of 2-methyl-2H-indazol-6-ylamine, 0.4 ml (3.68 mmol) of N-methylmorpholine and 0.729 g (1.92 mmol) of O-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluroniumhexafluorophosphate (HATU) in 25 ml of dimethylformamide are stirred for 16 hours at room temperature. The dimethylformamide is drawn off in an oil pump vacuum. The remaining residue is drawn off in saturated sodium bicarbonate solution. It is extracted three times with ethyl acetate, and the combined organic phases are dried, filtered and concentrated by evaporation. The residue is chromatographed on silica gel with a gradient that consists of hexane:acetone=100:0 to 50:50 as an eluant. 0.669 g (96% of theory) of 2-[(2-bromo-pyridin-4-ylmethyl)-amino]-N-(2-methyl-2H-indazol-6-yl)-benzamide is obtained in the form of a beige foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07615565B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-1427927cdc814fd3bf060e2632f8f30b
출처 메모uspto-grants-2009_11