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HRID 47238作成日:2026年10月25日

Formaldehyde → HCID 68835881、化合物

https://huagongshe.com/reaction/47238

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物1-MethylpiperazineHCID 53167—
反応物(Z)-3-((1H-pyrrol-2-yl)methylene)indolin-2-oneHCID 5908088—
溶媒EthanolHCID 702—
生成物HCID 68835881HCID 6883588121%

反応条件

温度0 °C

反応手順

A mixture of Z-(1H-Pyrrol-2-ylmethylene)-1,3-dihydro-indol-2-one (120 mg, 0.57 mmol), paraformaldehyde (17 mg, 0.57 mmol), and 1-methylpiperazine (63 μL, 0.57 mmol) in 4.0 mL EtOH was heated at reflux for 6.5 h. After standing at room temperature for 23 h, the mixture was concentrated to 3 mL solvent and 1 mL of hexane added. The resulting solution was cooled to 0° C. and the yellow solid which formed was collected by filtration. The solid collected was partitioned between 30 mL dilute HCl and 20 mL Ethyl acetate. The organic layer was removed and the aqueous layer washed with ethyl acetate (15 mL). The aqueous layer was made basic to pH 8 with saturated NaHCO3 and extracted with ethyl acetate. The ethyl acetate layer was washed with H2O, brine and dried with Na2SO4. The organic layer was concentrated and the residue was crystallized from ethyl acetate/hexane to give the title compound (38 mg, 21%) as a bright yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06699863B1
出典データセットuspto-grants-2004_03
ORD IDord-071b76b7dc524e829eb7e50af8cf8210
出典メモuspto-grants-2004_03