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HRID 1713966作成日:2026年10月27日

Phenacyl bromide → N-(3-Morpholinopropyl)-N-(4-phenylthiazol-2-yl)thiophene-2-carboxamide

https://huagongshe.com/reaction/1713966

反応式

関与物質

役割名称HCID仕込み量
反応物Phenacyl bromideHCID 6259—
反応物2-Thiophenecarbonyl chlorideHCID 78928—
反応物DiisopropylethylamineHCID 81531—
反応物N-[3-(4-Morpholinyl)propyl]thioureaHCID 2760135—
溶媒EthanolHCID 702—
生成物N-(3-Morpholinopropyl)-N-(4-phenylthiazol-2-yl)thiophene-2-carboxamideHCID 113951354%

反応手順

A mixture of 2-bromoacetophenone (60 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 (67 mg) as an off-white solid as the hydrochloride salt. LC/MS (ESI) m/z 413.9 [M+H]. HPLC retention time (Method A)=2.78 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-8c6a250449f84ef3b7d2990547fe1178
出典メモuspto-grants-2010_09