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HRID 515729作成日:2026年10月26日

Hydrochloric Acid → 7-Methoxy-8-methyl-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-one

https://huagongshe.com/reaction/515729

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Methyl AcrylateHCID 7294—
反応物TetrahydrofuranHCID 8028—
反応物ethyl 5-methoxy-4-methyl-1H-indole-2-carboxylateHCID 21396313—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TolueneHCID 1140—
生成物7-Methoxy-8-methyl-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-oneHCID 67249703—

反応手順

To a suspension of ethyl 5-methoxy-4-methyl-1H-indole-2-carboxylate (712 mg, 3.05 mmol) in toluene (10 mL) was added a 1 M solution of KOtBu in THF (3.97 mL, 3.97 mmol). The reaction mixture was stirred at room temperature for 5 min, methyl acrylate (825 μL, 9.15 mmol) was added. The reaction was stirred at reflux overnight and neutralized with 1 N HCl aqueous solution. The solid was collected and divided into three microwave vial. Each was added AcOH (8 mL) and H2O (1 mL), and heated at 180° C. for 15 min under microwave irradiation. The solvent was evaporated and the residue was purified by silica gel column chromatography to give the title compound as a yellow solid (500 mg). LCMS m/z=216.2 [M+H]+; 1H NMR (400 MHz, CDCl3) δ ppm 2.45 (s, 3H), 3.21 (t, J=6.5 Hz, 2H), 3.68 (s, 3H), 4.40 (t, J=6.2 Hz, 2H), 6.98 (s, 1H), 7.13 (d, J=9.0 Hz, 1H), 7.23 (d, J=9.0 Hz, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09108969B2
出典データセットuspto-grants-2015_08
ORD IDord-9662b9e604d14456a6dddab211201da2
出典メモuspto-grants-2015_08