戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 50114作成日:2026年10月26日

Methane → Losartan potassium salt

https://huagongshe.com/reaction/50114

反応式

関与物質

役割名称HCID仕込み量
反応物MethaneHCID 297—
反応物Potassium HydroxideHCID 14797—
反応物2-n-butyl-4-chloro 1-[(2'-(2-triphenylmethyl-2H-tetrazol-5-yl)-1,1'biphenyl-4-yl)-me thyl]-1H-imidazol-5-methanol methyl-isobutyl ketoneHCID 69886909—
溶媒MethanolHCID 887—
生成物Losartan potassium saltHCID 1147671095.9%

反応手順

Under nitrogen, in a 500 ml flask a mixture of 175 ml of dry methanol, 20 g (0.026 mol) of 2-n-butyl-4-chloro 1-[(2′-(2-triphenylmethyl-2H-tetrazol-5-yl)-1,1′biphenyl-4-yl)-me thyl]-1H-imidazol-5-methanol methyl-isobutyl ketone solvate and 1.46 g (0.026 mol) of potassium hydroxide in 25 ml of methanol was warmed to reflux temperature over a period of 30 min. After refluxing for 4 h, the reaction was cooled to room temperature, treated with 0.6 g of charcoal and filtered. The filtrate was concentrated to a volume of 30-35 ml under diminished pressure, and after addition of 85 ml of acetonitrile again to a volume of 30-35 ml. After addition of further 85 ml of acetonitrile the solution is concentrated to a volume of 60-65 ml. The suspension was stirred at 0−(+)2° C. for 2 h, the precipitated crystals were filtered, washed three times with 30 ml of cold acetonitrile and dried at 70° C. to give 11.5 g (94%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710183B2
出典データセットuspto-grants-2004_03
ORD IDord-6022181667ea4138a8f6aead0a43b0a4
出典メモuspto-grants-2004_03