참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 1-(2-Aminoethyl)-5,5-dimethylimidazolidine-2,4-dione | HCID 57428804 | — |
| 반응물 | 2-(5-Bromo-2-(methylsulfonyl)pyrimidin-4-yl)thiazolo[5,4-c]pyridine | HCID 60204372 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 생성물 | HCID 60204370 | HCID 60204370 | 5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07858785B2 |
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| 출처 데이터셋 | uspto-grants-2010_12 |
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| ORD ID | ord-d4b45daec7c0449cb09497deef58e910 |
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| 출처 메모 | uspto-grants-2010_12 |
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