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HRID 249922作成日:2026年10月26日

Methyl 2-amino-6-fluoro-3-hydroxybenzoate → Methyl 2-amino-5-fluorobenzoxazole-4-carboxylate

https://huagongshe.com/reaction/249922

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 2-amino-6-fluoro-3-hydroxybenzoateHCID 66873679—
反応物di(1H-imidazole-1-yl)methanamineHCID 66874404—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 2-amino-5-fluorobenzoxazole-4-carboxylateHCID 66873993—

反応手順

To a solution of methyl 2-amino-6-fluoro-3-hydroxybenzoate (0.4 g, 2.2 mmol) in THF (10 mL) was added di-(1H-imidazole-1-yl)methanamine (0.44 g, 2.75 mmol) at room temperature and the resulting reaction mixture was heated at reflux for 16 h. The reaction mixture cooled to room temperature and was concentrated under reduced pressure. The residue was dissolved in CH2Cl2 (100 mL), and the solution was treated with saturated aqueous ammonium chloride (25 mL). The organic layer was separated and the aqueous layer was extracted with additional 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 ether to afford methyl 2-amino-5-fluorobenzoxazole-4-carboxylate. 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-eaa3a55acb134139bc55aedf3f9b9501
出典メモuspto-grants-2011_01