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HRID 1086854作成日:2026年10月26日

Oxalyl chloride → 1-(Indole-5-carbonyl)-4-phenethylpiperazine

https://huagongshe.com/reaction/1086854

反応式

関与物質

役割名称HCID仕込み量
反応物Oxalyl chlorideHCID 65578—
反応物1H-Indole-5-Carboxylic AcidHCID 74280—
反応物1-PhenethylpiperazineHCID 79214—
反応物DiisopropylethylamineHCID 81531—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物1-(Indole-5-carbonyl)-4-phenethylpiperazineHCID 14985997—

反応手順

Indole-5-carboxylic acid (57 mg, 0.35 mmol) was dissolved in THF(2 ml) and DMF (1 drop), then oxalyl chloride (37 μl, 54 mg, 0.42 mmol) was added. The mixture was stirred at room temperature for 3 hours, the solvent was evaporated under reduced pressure and the residue was dissolved in DMF (2 ml) and added to a stirred solution of 1-phenethylpiperazine (66 mg, 0.35 mmol) and diisopropylethylamine (91 μl, 68 mg, 0.52 mmol) in dichloromethane (1 ml). The mixture was stirred at room temperature for 24 hours, then the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with CH2Cl2 /CH3OH/NH3 ; 95:5:0.5 and crystallized from EtOAc/hexane to give the piperazine as microcrystals (32 mg, 27%), mp 105°-108° C. δH (CDCl3) 8.47(1H, br s), 7.73(1H, s), 7.38(1H, d J 8.4 Hz), 7.32-7.19(7H, m), 6.56(1H, br s), 3.7(4H, br s), 2.81(2H, m), 2.65(2H, m), and 2.6(4H, br s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05032598
出典データセットuspto-grants-1991_07
ORD IDord-c62a4b98bde34dbd84a8225a42a4089e
出典メモuspto-grants-1991_07