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HRID 352295作成日:2026年10月25日

Formaldehyde → 1-Butylaminomethyl-3-(1H-pyrrol-2-ylmethylene)-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/352295

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物ButylamineHCID 8007—
反応物HexaneHCID 8058—
反応物(Z)-3-((1H-pyrrol-2-yl)methylene)indolin-2-oneHCID 5908088—
溶媒EthanolHCID 702—
生成物1-Butylaminomethyl-3-(1H-pyrrol-2-ylmethylene)-1,3-dihydro-indol-2-oneHCID 68834641—

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 (120.0 mg, 0.571 mmol), paraformaldehyde (17.1 mg, 0.571 mmol), and butylamine (56.4 μL, 0.571 mmol) in 5.5 mL of EtOH was heated at reflux for 2.5 h. Then reaction mixture was treated with 2 mL of hexane was and then cooled to 0° C. The reaction mixture was then filtered to remove Z-(1H-Pyrrol-2-ylmethylene)-1,3-dihydro-indol-2-one. The filtrate was partitioned between dilute HCl and ethyl acetate. The organic layer was removed and the aqueous layer washed with 15 mL Ethyl acetate. The aqueous phase 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 over anhydrous Na2SO4. The solvent was removed in vacuo to give 58 mg of yellow oil. The oil was purified by chromatography (silica gel, 1:1/hexane:ethyl acetate) to give the title compound (51.6 mg, 31%) as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06747025B1
出典データセットuspto-grants-2004_06
ORD IDord-3c43b2fd8cd84d0998e9183c24fbc01f
出典メモuspto-grants-2004_06