戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 591713作成日:2026年10月25日

4-Methylmorpholine → 2-Amino-6-methoxybenzamide

https://huagongshe.com/reaction/591713

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethylmorpholineHCID 7972—
反応物Ammonium HydroxideHCID 14923—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物2-Amino-6-methoxybenzoic AcidHCID 2735357—
溶媒TetrahydrofuranHCID 8028—
生成物2-Amino-6-methoxybenzamideHCID 12264814—

反応手順

To a stirred solution of 2-amino-6-methoxy-benzoic acid (3.00 g, 17.9 mmol) in THF (90 mL), EDCl (7.89 g, 41.1 mmol) and HOBt (7.95 g, 51.9 mmol) were added and stirred at room temperature for 30 minutes then N-methylmorpholine (6.15 g, 60.0 mmol) and aqueous 50% v/v NH4OH (12 mL, 171.4 mmol) was added. The mixture was stirred for 16 hours at room temperature. The solvent was removed under reduced pressure and the residue was extracted with ethylacetate (4×100 mL), the combined organic phase was washed with water and brine, and dried over anhydrous sodium sulfate; the solvent was evaporated to give 2-amino-6-methoxy-benzamide as an off-white solid. Yield: 1.90 g, (65%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09238640B2
出典データセットuspto-grants-2016_01
ORD IDord-5433fdcfe75c4111bad2426fabcc7433
出典メモuspto-grants-2016_01