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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

반응식

참여 물질

역할이름HCID투입량
반응물2-Thiophenecarbonyl chlorideHCID 78928—
반응물DiisopropylethylamineHCID 81531—
반응물N-[3-(4-Morpholinyl)propyl]thioureaHCID 2760135—
반응물2-Bromo-1-(2,3-dihydro-1,4-benzodioxin-6-yl)ethan-1-oneHCID 2776171—
용매EthanolHCID 702—
생성물N-(4-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)thiazol-2-yl)-N-(3-morpholinopropyl)thiophene-2-carboxamideHCID 6840616650.9%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07410988B2
출처 데이터셋uspto-grants-2008_08
ORD IDord-524616086db74ea3998d5cafb08506e6
출처 메모uspto-grants-2008_08