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HRID 7629作成日:2026年10月24日

Tetrahydrofuran → 2-[7-(3-Fluoro-benzyloxy)-2-methyl-4-oxo-4H-quinazolin-3-yl]-acetamide

https://huagongshe.com/ja/reaction/7629

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Sodium HydroxideHCID 14798—
反応物Lithium hydroxide, monohydrateHCID 168937—
反応物4-(3-Fluoro-benzyloxy)-2-nitro-benzoic acidHCID 21991771—
反応物4-(3-Fluoro-benzyloxy)-2-nitro-benzoic acid methyl esterHCID 69594337—
反応物4-(3-Fluorobenzyloxy)-2-nitro-benzoic acid (3-fluoro-benzyl) esterHCID 86593646—
溶媒WaterHCID 962—
生成物2-[7-(3-Fluoro-benzyloxy)-2-methyl-4-oxo-4H-quinazolin-3-yl]-acetamideHCID 1002018065%

反応手順

4-(3-Fluoro-benzyloxy)-2-nitro-benzoic acid: A mixture of 4-(3-fluorobenzyloxy)-2-nitro-benzoic acid (3-fluoro-benzyl) ester and 4-(3-fluoro-benzyloxy)-2-nitro-benzoic acid methyl ester (14.0 g, 35.0 mmol) in THF (120 mL) and water (120 mL), containing lithium hydroxide monohydrate (2.94 g, 70.1 mmol) was stirred at rt for 48 h. Then the mixture was poured into sodium hydroxide (2 N, 50 mL) and then the mixture extracted with diethyl ether (3×150 mL). The aqueous phase was then adjusted to pH 2 with HCl. Then the mixture was poured into sodium hydroxide (2 N, 50 mL) and the aqueous phase was then adjusted to pH 5.2 with HCl then the mixture extracted with diethyl ether (3×100 mL). The combined extracts were then washed with brine (100 mL) dried and evaporated to afford title compound (6.6 g, 65%) as a light yellow solid. MS: m/e=290.0 (M−H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087612B2
出典データセットuspto-grants-2006_08
ORD IDord-ad3689421b0444ecba177dceb56a6917
出典メモuspto-grants-2006_08