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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 577429생성일: 2026년 10월 24일

(R)-2-amino-3-methylbutanamide → 5-((1-methyl-1H-indol-4-yl)amino)-3-(((5-oxopyrrolidin-2-yl)methyl)amino)-1,2,4-triazine-6-carboxamide

https://huagongshe.com/ko/reaction/577429

반응식

참여 물질

역할이름HCID투입량
반응물(R)-2-amino-3-methylbutanamideHCID 444079—
반응물5-(Aminomethyl)pyrrolidin-2-oneHCID 14143189—
반응물(R)-3-((1-amino-3-methyl-1-oxobutan-2-yl)amino)-5-((1-methyl-1H-indol-4-yl)amino)-1,2,4-triazine-6-carboxamideHCID 86706423—
생성물5-((1-methyl-1H-indol-4-yl)amino)-3-(((5-oxopyrrolidin-2-yl)methyl)amino)-1,2,4-triazine-6-carboxamideHCID 86706422—

반응 단계

The title compound was prepared in a similar procedure as described in Example (R)-3-((1-amino-3-methyl-1-oxobutan-2-yl)amino)-5-((1-methyl-1H-indol-4-yl)amino)-1,2,4-triazine-6-carboxamide. Here though, 5-(aminomethyl)pyrrolidin-2-one was utilized instead of (R)-2-amino-3-methylbutanamide. MS found for C18H20N8O2 as (M+H)+ 381.3. UV: λ=219, 239, 292 nm. Proton NMR: (CD3OD) δ 7.90 (1H, d, J=8.0 Hz), 7.36-7.22 (3H, m), 6.60 (1H, dd, J=0.8 Hz, 2.8 Hz), 3.98 (1H, m), 3.84 (3H, s), 3.62-3.51 (2H, m), 2.40, −2.20 (3H, m), 1.90 (1H, m) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09040530B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-9f1d139deb72439c83c98d1fa749157b
출처 메모uspto-grants-2015_05