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HRID 1085997作成日:2026年10月26日

Salbutamol → Methyl-5[[(1,1-dimethylethyl)(phenylmethyl)-amino]acetyl]-2-hydroxybenzoate

https://huagongshe.com/reaction/1085997

反応式

関与物質

役割名称HCID仕込み量
反応物SalbutamolHCID 2083—
反応物AcetophenoneHCID 7410—
反応物N-(1,1-Dimethylethyl)benzenemethanamineHCID 76908—
反応物Bromoacetyl-2-hydroxybenzoateHCID 21684415—
生成物Methyl-5[[(1,1-dimethylethyl)(phenylmethyl)-amino]acetyl]-2-hydroxybenzoateHCID 12814682—

反応手順

Albuterol has been prepared, see Irish Patent Specification No. 31391, Aug. 9, 1972, starting from the appropriate acetophenone derivative methyl-5-(bromoacetyl-2-hydroxybenzoate, by condensation with N-(1,1-dimethylethyl)benzenemethanamine in the presence of base to form the ketonic ester, methyl-5[[(1,1-dimethylethyl)(phenylmethyl)-amino]acetyl]-2-hydroxybenzoate. The ketonic ester is reduced with lithium aluminum hydride in tetrahydrofuran under nitrogen to yield α1 -[[(1,1-dimethylethyl)-(phenylmethyl)amino]methyl]-4-hydroxy-1,3-benzenedimethanol which is subsequently debenzylated with hydrogen in the presence of palladium on carbon catalyst to produce albuterol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05011993
出典データセットuspto-grants-1991_04
ORD IDord-5b8dcbadf97f4773909981ee451ff8e5
出典メモuspto-grants-1991_04