Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18920생성일: 2026년 10월 25일
1,2-Dichloro-3-isocyanatobenzene → 1-(5-Tert-butyl-3-(2-ethyl-2-methyl-3-oxopiperazine-1-carbonyl)thiophen-2-yl)-3-(2,3-dichlorophenyl)urea
https://huagongshe.com/reaction/18920
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,2-Dichloro-3-isocyanatobenzene | HCID 33050 | — |
| 반응물 | HCID 58679278 | HCID 58679278 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-(5-Tert-butyl-3-(2-ethyl-2-methyl-3-oxopiperazine-1-carbonyl)thiophen-2-yl)-3-(2,3-dichlorophenyl)urea | HCID 58679326 | 44.4% |
반응 단계
To 4-(2-amino-5-tert-butylthiophene-3-carbonyl)-3-ethyl-3-methylpiperazin-2-one (72.0 mg, 0.22 mmol) in THF (2 mL) was added 1,2-dichloro-3-isocyanatobenzene (50.0 mg, 0.27 mmol). The resulting reaction mixture was stirred at room temperature and the reaction progress monitored by SFC-MS. When the reaction was completed, solvent was removed under reduced pressure and the crude product purified by preparative TLC to afford 1-(5-tert-butyl-3-(2-ethyl-2-methyl-3-oxopiperazine-1-carbonyl)thiophen-2-yl)-3-(2,3-dichlorophenyl)urea (50 mg, 44%) as pale yellow solid. 1H NMR (400 MHz, DMSO-d6): δ (ppm) 9.93 (s, 1H), 9.52 (s, 1H), 8.10 (s, 1H), 7.86 (d, J=8.2 Hz, 1H), 7.26-7.22 (m, 2H), 6.46 (s, 1H), 3.62-3.58 (m, 1H), 3.40-3.35 (m, 1H), 3.30-3.23 (m, 1H), 3.19-3.13 (m, 1H), 2.65-2.61 (m, 1H), 1.89-1.85 (m, 1H), 1.58 (s, 3H), 1.22 (s, 9H), 0.69 (t, J=7.4 Hz, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07741479B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-d48686ac2ea74bda8f3f416086f00a52 |
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| 출처 메모 | uspto-grants-2010_06 |
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