Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2218504생성일: 2026년 10월 25일
2-Thiophenecarbonyl chloride → N-(4-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)thiazol-2-yl)-N-(3-morpholinopropyl)thiophene-2-carboxamide
https://huagongshe.com/reaction/2218504
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 2-Thiophenecarbonyl chloride | HCID 78928 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | N-[3-(4-Morpholinyl)propyl]thiourea | HCID 2760135 | — |
| 반응물 | 2-Bromo-1-(2,3-dihydro-1,4-benzodioxin-6-yl)ethan-1-one | HCID 2776171 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | N-(4-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)thiazol-2-yl)-N-(3-morpholinopropyl)thiophene-2-carboxamide | HCID 68406166 | 50.9% |
반응 단계
A mixture of 3,4-(ethylenedioxy)phenacyl bromide (77 mg, 0.3 mmol) and (3-morpholin-4-yl-propyl)-thiourea (61 mg, 0.3 mmol) in dry ethanol (3 mL) was heated at reflux for 10 min, cooled to room temperature, and concentrated in vacuo. The resulting residue was suspended in dichloromethane (3 mL) followed by the addition of N,N-diisopropylethylamine (105 μL, 0.6 mmol) and thiophene-2-carbonyl chloride (34 μL, 0.32 mmol). The reaction mixture was maintained at room temperature overnight, then concentrated in vacuo. The resulting residue was dissolved in DMSO (1.5 mL) and subjected to HPLC purification (Method Y). The resulting free amine was dissolved in MeOH (1 mL) and 1M HCl/ether (50 mL) was added. The precipitate was filtered and dried in vacuo to provide the title compound (72 mg) as an off-white solid as the hydrochloride salt. LC/MS (ESI) m/z 472.3 [M+H]. HPLC retention time (Method A)=2.72 min.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07410988B2 |
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| 출처 데이터셋 | uspto-grants-2008_08 |
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| ORD ID | ord-524616086db74ea3998d5cafb08506e6 |
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| 출처 메모 | uspto-grants-2008_08 |
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