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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14997생성일: 2026년 10월 24일

Diisopropylethylamine → 2-(5,5-Dioxo-5,10-dihydrophenothiazin-2-yl)-n-(1-methyl-1h-pyrazol-3-yl)-3-(tetrahydropyran-4-yl)propionamide

https://huagongshe.com/ko/reaction/14997

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1-Methyl-3-aminopyrazoleHCID 137254—
반응물HOAtHCID 181649—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물2-(5,5-Dioxo-5,10-dihydrophenothiazin-2-yl)-3-(tetrahydropyran-4-yl)propionic acidHCID 58024229—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물2-(5,5-Dioxo-5,10-dihydrophenothiazin-2-yl)-n-(1-methyl-1h-pyrazol-3-yl)-3-(tetrahydropyran-4-yl)propionamideHCID 58024260—

반응 단계

600 mg of 2-(5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-3-(tetrahydropyran-4-yl)propionic acid, 120 mg of commercially available 1-methyl-1H-pyrazole-3-amine and 729 μl of N,N-diisopropylethylamine are dissolved in 5 ml of dimethylformamide. 561 mg of HATU and 200 mg of HOAT are added, and the mixture is stirred at room temperature for two hours. The reaction mixture is then diluted by addition of 200 ml of ethyl acetate and washed three times with in each case 50 ml of water and saturated sodium chloride solution. The organic phase is dried over MgSO4, and the solvent is then removed under reduced pressure. The residue is purified by RP-HPLC. This gives 200 mg of 2-(5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-N-(11-methyl-1H-pyrazol-3-yl)-3-(tetrahydropyran-4-yl)propionamide as a colorless lyophilisate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732440B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-6d934af18b0a4f2baa267241da828b8e
출처 메모uspto-grants-2010_06