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HRID 249921作成日:2026年10月24日

Methyl 2-amino-3-hydroxy-5-methylbenzoate → Methyl 2-amino-6-methylbenzoxazole-4-carboxylate

https://huagongshe.com/ja/reaction/249921

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 2-amino-3-hydroxy-5-methylbenzoateHCID 21755136—
反応物di(1H-imidazole-1-yl)methanamineHCID 66874404—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 2-amino-6-methylbenzoxazole-4-carboxylateHCID 6687443345%

反応手順

To a solution of di (1H-imidazole-1-yl)methanamine (1.56 g, 9.67 mmol) in THF (30 mL) was added methyl 2-amino-3-hydroxy-5-methylbenzoate (1.40 g, 7.73 mmol) at room temperature and the resulting reaction mixture was heated at reflux for 6 h. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The residue was dissolved in CH2Cl2 (100 mL), treated with saturated aqueous ammonium chloride (25 mL), and then extracted with CH2Cl2 (2×100 mL). The combined organic phase was washed with brine (2×100 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure to afford a yellow solid. The solid was triturated from CH3OH to afford methyl 2-amino-6-methylbenzoxazole-4-carboxylate (0.717 g, 45%). 1H NMR and MS consistent.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07863271B2
出典データセットuspto-grants-2011_01
ORD IDord-1e57ef9aef8b42c0acadced7b7b9d7e4
出典メモuspto-grants-2011_01