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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19513생성일: 2026년 10월 23일

2-Pyrazinecarboxylic acid → Pyrazine-2-carboxylic acid 4-(4-amino-2-methyl-quinolin-6-ylcarbamoyl)-benzylamide

https://huagongshe.com/ko/reaction/19513

반응식

참여 물질

역할이름HCID투입량
반응물2-Pyrazinecarboxylic acidHCID 1047—
반응물EthylmorpholineHCID 7525—
반응물O-[(Ethoxycarbonyl)cyanomethylenamino]-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733286—
반응물4-Aminomethyl-N-(4-amino-2-methyl-quinolin-6-yl)-benzamideHCID 17864623—
용매DimethylformamideHCID 6228—
생성물Pyrazine-2-carboxylic acid 4-(4-amino-2-methyl-quinolin-6-ylcarbamoyl)-benzylamideHCID 12110091111.2%

반응 단계

To a solution of 10.5 mg (0.08 mmol) of 2-pyrazinecarboxylic acid in 1 ml of DMF were added 27.9 mg (0.085 mmol) TOTU. After 15 min at room temperature 55 mg (0.085 mmol) of 4-Aminomethyl-N-(4-amino-2-methyl-quinolin-6-yl)-benzamide and 39 mg (0.34 mmol) of N-ethylmorpholine were added. After 24 h stirring at room temperature the solution was evaporated and the residue was treated with acetonitrile and water containing 0.005% trifluoroacetic acid. The precipitate was filtered to give 36.7 mg (71%) of the title compound. MS 413.42 (M+1)+, 1H-NMR (DMSO-d6) δ 2.58 (s, 3H), 4.60 (d, 2H), 6.58 (s, NH), 7.55 (d, 2H), 7.81 (d, 1H), 8.00 (m, 3H), 8.65 (br.s., NH2), 8.78 (m, 2H), 8.90 (m, 1H), 9.20 (s, 1H), 9.62 (m, 1H), 10.80 (s, NH), 13.38 (br.s., NH).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745443B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-e4b1890606394513a607daaa28ddf54f
출처 메모uspto-grants-2010_06