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HRID 1465267作成日:2026年10月25日

Triethylamine → 5-(2-fluorophenethyl)-2,3,4,5-tetrahydro-8-iodo-2-methyl-1H-pyrido[4,3-b]indole

https://huagongshe.com/reaction/1465267

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物TrifluoroacetateHCID 84468—
反応物2-Fluorophenethyl bromideHCID 2756964—
反応物4-Iodophenylhydrazine hydrochlorideHCID 12208795—
反応物1-Methylpiperidin-4-one hydrochlorideHCID 12210057—
溶媒EthanolHCID 702—
生成物5-(2-fluorophenethyl)-2,3,4,5-tetrahydro-8-iodo-2-methyl-1H-pyrido[4,3-b]indoleHCID 578762460.5%

反応手順

Preparation of the title compound was carried out according to General Method 8. 4-Iodophenylhydrazine hydrochloride (500 mg, 2.1 mmol), 2-fluorophenethylbromide (0.3 ml, 2.1 mmol), triethyl amine (0.8 ml, 6.3 mmol) and N-methyl-4-piperidone hydrochloride (312 mg, 2.1 mmol) were taken in ethanol (10 ml) to obtain 5 mg of 5-(2-fluorophenethyl)-2,3,4,5-tetrahydro-8-iodo-2-methyl-1H-pyrido[4,3-b]indole as a trifluoroacetate salt after purification by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in Water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 mL).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08999978B2
出典データセットuspto-grants-2015_04
ORD IDord-0a95e1a5e4714435b028873f49450039
出典メモuspto-grants-2015_04