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HRID 388318作成日:2026年10月26日

2-Naphthoic acid → N-(2-(methoxy(methyl)amino)-2-oxoethyl)-2-naphthamide

https://huagongshe.com/reaction/388318

反応式

関与物質

役割名称HCID仕込み量
反応物2-Naphthoic acidHCID 7123—
反応物DiisopropylethylamineHCID 81531—
反応物Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
反応物Sodium BicarbonateHCID 516892—
反応物2-amino-N-methoxy-N-methylacetamideHCID 10329278—
溶媒DichloromethaneHCID 6344—
生成物N-(2-(methoxy(methyl)amino)-2-oxoethyl)-2-naphthamideHCID 45866900—

反応手順

To a mixture of 2-naphthoic acid (5.8 g, 33.7 mmol), 2-amino-N-methoxy-N-methylacetamide (Gly Weinreb amide; prepared from Boc-Gly Weinreb amide 15 as in Example 43) (3.8 g, 32.1 mmol) and DIPEA (12.0 mL, 68.9 mmol) in DCM (70 mL) was added BOP (14.9 g, 33.7 mmol) in one portion at room temperature. The resulting mixture was stirred for 1 hr then saturated NaHCO3 aqueous solution was added. The organic layer was washed with brine (5×60 mL) and 1 N HCl (2×30 mL), dried over MgSO4, filtered and concentrated under reduced pressure to give the crude product, which was used in the next reaction without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08377925B2
出典データセットuspto-grants-2013_02
ORD IDord-7df3c81b3498407581b4ed714b3e0b1d
出典メモuspto-grants-2013_02