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HRID 49462作成日:2026年10月25日

2-Naphthalenesulfonyl chloride → N-(2-{[(3-Hydroxypropyl)amino]methyl}-3,4-dihydro-2H-chromen-7-yl)naphthalene-2-sulfonamide

https://huagongshe.com/reaction/49462

反応式

関与物質

役割名称HCID仕込み量
反応物2-Naphthalenesulfonyl chlorideHCID 7125—
反応物3-Amino-1-propanolHCID 9086—
反応物(7-Aminochroman-2-yl)methanolHCID 10511549—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
生成物N-(2-{[(3-Hydroxypropyl)amino]methyl}-3,4-dihydro-2H-chromen-7-yl)naphthalene-2-sulfonamideHCID 10202719—

反応条件

温度80 °C

反応手順

A solution of (7-amino-3,4-dihydro-2H-chromen-2-yl)methanol (25 mg, 140 μmol) in pyridine is treated with 2-naphthalenesulfonylchloride (70 mg, 308 μmol) at ambient temperature for 1 h, treated with 3-amino-1-propanol (3 mmol, 0.23 mL), heated at 80° C. for 3 h, diluted with water and extracted with ethyl acetate. The extracts are combined, dried over Na2SO4 and concentrated in vacuo. The resultant residue is purified by reverse phase preparative HPLC to give the title product, M+H 427, retention time 7.92 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06706757B2
出典データセットuspto-grants-2004_03
ORD IDord-b252316eb42d4f76a074015cae6cf308
出典メモuspto-grants-2004_03