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HRID 1713972作成日:2026年10月26日

2-Thiophenecarbonyl chloride → N-(3-Morpholinopropyl)-N-(4-(3-phenylisoxazol-5-yl)thiazol-2-yl)thiophene-2-carboxamide

https://huagongshe.com/reaction/1713972

反応式

関与物質

役割名称HCID仕込み量
反応物2-Thiophenecarbonyl chlorideHCID 78928—
反応物DiisopropylethylamineHCID 81531—
反応物5-(Bromoacetyl)-3-phenylisoxazoleHCID 2735532—
反応物N-[3-(4-Morpholinyl)propyl]thioureaHCID 2760135—
溶媒1,4-DioxaneHCID 31275—
生成物N-(3-Morpholinopropyl)-N-(4-(3-phenylisoxazol-5-yl)thiazol-2-yl)thiophene-2-carboxamideHCID 5976968953.8%

反応条件

温度80 °C

反応手順

A mixture of 2-bromo-1-(3-phenylisoxazol-5-yl)ethan-1-one (160 mg, 0.6 mmol) and (3-morpholin-4-yl-propyl)-thiourea (122 mg, 0.6 mmol) in dry dioxane (5 ml) was heated at 80° C. for 2 h, cooled to room temperature, and concentrated in vacuo. The resulting residue was suspended in dichloromethane (5 mL) followed by the addition of N,N-diisopropylethylamine (209 μL, 1.2 mmol) and thiophene-2-carbonyl chloride (96 μL, 0.9 mmol). The reaction mixture was maintained at room temperature overnight, then concentrated in vacuo. The resulting residue was dissolved in DMSO (2.5 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 (155 mg) as an off-white solid as the hydrochloride salt. LC/MS (ESI) m/z 481.1 [M+H]. HPLC retention time (Method B)=2.94 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07795290B2
出典データセットuspto-grants-2010_09
ORD IDord-0d95d6129f614471822fbaaf9c876d53
出典メモuspto-grants-2010_09