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HRID 261896作成日:2026年10月27日

Hydrochloric Acid → Albendazole

https://huagongshe.com/reaction/261896

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Methyl chloroformateHCID 6586—
反応物CyanamideHCID 9864—
反応物Sodium HydroxideHCID 14798—
反応物4-(Propylthio)benzene-1,2-diamineHCID 3017084—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物AlbendazoleHCID 2082—

反応条件

温度50 °C

反応手順

Preparation of methyl 5-propylthio-2-benzimidazole carbamate--A 1.82 g portion of cyanamide was dissolved in 10 ml of water. Methyl chloroformate, 4.64 g, and 6.34 g of 50% aqueous sodium hydroxide in 6 ml of water were added simultaneously so as to maintain the pH at approximately 7 as determined by a pH meter. The reaction mixture was stirred at 50° C. for one hour. A portion of 7.4 g of concentrated hydrochloric acid in 7 ml of water was added until the pH was 4. The methanol solution of 4-propylthio-o-phenylenediamine from Example IV was added at once. More of the hydrochloric acid solution was added to adjust the pH to 4. The reaction mixture was heated to distill the methanol. As methanol was nearly removed more hydrochloric acid solution was added to keep the pH at 4. Water was added from time to time to keep the slurry from becoming too thick. The reaction slurry was heated at 100° C. for one hour after the methanol had been removed. The reaction slurry was cooled, filtered and washed liberally with water. The solids were air dried to produce 8.77 g of crude methyl 5-propylthio-2-benzimidazole carbamate. The crude solids were washed 3 times with cold acetone and dried to produce 7.52 g of product assaying 97% methyl-5-propylthio-2-benzimidazole carbamate by HPLC, 73% yield from the 4-propylthio-2-nitroaniline employed in Example IV.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04152522
出典データセットuspto-grants-1979_05
ORD IDord-5c65760cded345e7878fe56986be3995
出典メモuspto-grants-1979_05