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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1297440생성일: 2026년 10월 24일

N-Methyl-N-[(2-methyl-1H-indol-3-yl)methyl]amine → (E)-3-(3,4-dihydro-2H-pyrido[3,2-b]-1,4-oxazin-7-yl)-N-methyl-N-(1-methyl-1H-indol-3-ylmethyl)acrylamide

https://huagongshe.com/ko/reaction/1297440

반응식

참여 물질

역할이름HCID투입량
반응물N-Methyl-N-[(2-methyl-1H-indol-3-yl)methyl]amineHCID 10954023—
반응물1-Methyl-3-(methylaminomethyl)indoleHCID 10986778—
반응물(E)-3-(3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazin-7-yl)acrylic acidHCID 22139122—
반응물(e)-3-(2-Oxo-2,3-dihydro-1h-indol-5-yl)acrylic acid hydrochloride saltHCID 66905016—
생성물(E)-3-(3,4-dihydro-2H-pyrido[3,2-b]-1,4-oxazin-7-yl)-N-methyl-N-(1-methyl-1H-indol-3-ylmethyl)acrylamideHCID 1004419383.3%

반응 단계

According to the procedure of Example 4, except substituting (E)-3-(3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazin-7-yl)acrylic acid (0.11 g, 0.53 mmole), from Preparation 7, for the (E)-3-(2-oxo-2,3-dihydro-1H-indol-5-yl)acrylic acid hydrochloride salt, and substituting 1-methyl-3-(methylaminomethyl) indole (0.10 g, 0.59 mmole) for the 2-methyl-3-(methylaminomethyl)-1H-indole, the title compound (0.16 g, 82%) was prepared as a light yellow solid: MS (ES) m/e 363 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07250424B2
출처 데이터셋uspto-grants-2007_07
ORD IDord-593fd79b2d774aa7ab8ca8fc7d57620a
출처 메모uspto-grants-2007_07