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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 261896생성일: 2026년 10월 26일

Hydrochloric Acid → Albendazole

https://huagongshe.com/reaction/261896

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Methyl chloroformateHCID 6586—
반응물CyanamideHCID 9864—
반응물Sodium HydroxideHCID 14798—
반응물4-(Propylthio)benzene-1,2-diamineHCID 3017084—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물AlbendazoleHCID 2082—

반응 조건

온도50 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04152522
출처 데이터셋uspto-grants-1979_05
ORD IDord-5c65760cded345e7878fe56986be3995
출처 메모uspto-grants-1979_05