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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2267321생성일: 2026년 10월 26일

Diisopropylethylamine → HCID 60204370, 화합물

https://huagongshe.com/reaction/2267321

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1-(2-Aminoethyl)-5,5-dimethylimidazolidine-2,4-dioneHCID 57428804—
반응물2-(5-Bromo-2-(methylsulfonyl)pyrimidin-4-yl)thiazolo[5,4-c]pyridineHCID 60204372—
용매IsopropanolHCID 3776—
생성물HCID 60204370HCID 602043705%

반응 조건

온도160 °C

반응 단계

A microwave tube was charged with 2-(5-bromo-2-(methylsulfonyl)pyrimidin-4-yl)thiazolo[5,4-c]pyridine (300 mg, 0.81 mmol), 1-(2-Aminoethyl)-5,5-dimethyl-imidazolidine-2,4-dione (138 mg, 0.81 mmol), isopropanol (3 mL) and N,N-diisopropylethylamine (0.21 mL, 1.21 mmol). The vessel was sealed and heated in a microwave reactor at 160° C. for 1000 seconds. The resulting solid was filtered off and washed with methanol (4×10 mL). The solid was then dissolved in dimethylsulfoxide (4 mL) and purified by reverse phase HPLC. Product fractions were combined and loaded onto an SCX cartridge, washed with methanol (4 mL), then free based and eluted with 2 M ammonia in methanol (4 mL). The solvent was evaporated in vacuo to yield 1-(2-(5-bromo-4-(thiazolo[5,4-c]pyridin-2-yl)pyrimidin-2-ylamino)ethyl)-5,5-dimethylimidazolidine-2,4-dione (17 mg, 5%) as a yellow amorphous solid. 1H NMR 6 (d6-DMSO, 400 MHz) 1.50 (s, 6 H), 3.67 (br. s., 2 H), 3.75 (br. s., 2 H), 4.32 (br. s., 1 H), 6.89 (s, 1 H), 7.49 (s, 1 H), 8.33 (d, J=5.5 Hz, 1 H), 8.91 (d, J=5.1 Hz, 1 H), 9.71 (s, 1 H): HRMS (M+H)+ Calcd. C17H16BrN7O2S 462.0348, found 462.0339.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07858785B2
출처 데이터셋uspto-grants-2010_12
ORD IDord-d4b45daec7c0449cb09497deef58e910
출처 메모uspto-grants-2010_12