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HRID 2230923作成日:2026年10月27日

Ammonium Hydroxide → Citalopram

https://huagongshe.com/reaction/2230923

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium HydroxideHCID 14923—
反応物Thionyl ChlorideHCID 24386—
反応物SulfamideHCID 82267—
反応物1-(3-(dimethylamino)propyl)-1-(4-fluorophenyl)-1,3-dihydro-5-Isobenzofurancarboxylic acidHCID 9928044—
溶媒WaterHCID 962—
溶媒HeptaneHCID 8900—
溶媒SulfolaneHCID 31347—
生成物CitalopramHCID 2771—

反応条件

温度130 °C

反応手順

5-Carboxy-1-(4-fluorophenyl)-1-(3-dimethylaminopropyl)-1,3-dihydro-isobenzofuran (5 g, 0.015 mole) and sulfamide (1.65 g, 0.017 mole) were dissolved in sulfolane (15 mL). Thionylchloride (2.25 g, 0.019 mole) was added at room temperature and the temperature of the reaction mixture was raised to 130° C. for 2 hours. The reaction mixture was allowed to cool to 75° C. and water (25 mL) was added. The temperature was held at 75° C. for 15 min, and then the reaction mixture was cooled to room temperature. pH was ajusted to 9 with ammonium hydroxide and then n-heptane (75 mL) was added. The temperature was raised to 70° C. and the hot n-heptane layer was isolated from which the title compound crystallised on cooling. Yield 3.77 g. Purity (HPLC peak area)>97%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06426422B1
出典データセットuspto-grants-2002_07
ORD IDord-88300376b7be48dc9e3b2271621cbed7
出典メモuspto-grants-2002_07