Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1161645생성일: 2026년 10월 25일
Diisopropylethylamine → (+/-) N-(3-{[2-(12,12-Dioxo-12lambda6-thia-tricyclo[6.3.1.02.7]dodeca-2(7),3,5-trien-4-ylamino)-5-trifluoromethyl-pyrimidin-4-ylamino]-methyl}-pyridin-2-yl)-N-methyl-methanesulfonamide
https://huagongshe.com/reaction/1161645
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | N-(3-(aminomethyl)pyridin-2-yl)-N-methylmethanesulfonamide | HCID 45480403 | — |
| 반응물 | (+/-) (4-Chloro-5-trifluoromethyl-pyrimidin-2-yl)-(12,12-dioxo-12lambda6-thia-tricyclo[6.3.1.02.7]dodeca-2(7),3,5-trien-4-yl)-amine | HCID 86761198 | — |
| 용매 | Dichloroethane t-butanol | HCID 86704321 | — |
| 생성물 | (+/-) N-(3-{[2-(12,12-Dioxo-12lambda6-thia-tricyclo[6.3.1.02.7]dodeca-2(7),3,5-trien-4-ylamino)-5-trifluoromethyl-pyrimidin-4-ylamino]-methyl}-pyridin-2-yl)-N-methyl-methanesulfonamide | HCID 59518908 | 18% |
반응 단계
A mixture of C6 (51 mg; 0.126 mmol) and 1:1 (vol:vol) t-BuOH/dichloroethane (500 μL) was added to a mixture of N-(3-Aminomethyl-pyridin-2-yl)-N-methyl-methanesulfonamide (38 mg, 0.139 mmol) and diisopropyl ethylamine (66 μL, 0.378 mmol). The reaction mixture was heated to 85° C. in a sealed vial. After two hours, the hot reaction mixture was loaded directly onto silica under reduced pressure, purified via chromatography (99:1:0.1 CHCl3:CH3OH:NH4OH), and concentrated under reduced pressure to provide 1 as a white solid (13 mg, 0.0223 mmol, 18%). LC/MS (Method F) r.t.=2.26 min.; m/z 583.2. HPLC r.t.=6.40 min.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07820648B2 |
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| 출처 데이터셋 | uspto-grants-2010_10 |
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| ORD ID | ord-98a7861602504b46a4637384b2933871 |
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| 출처 메모 | uspto-grants-2010_10 |
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