돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1720101생성일: 2026년 10월 24일

Hydrochloric Acid → Terazosin Hydrochloride Anhydrous

https://huagongshe.com/ko/reaction/1720101

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-MethoxyethanolHCID 8019—
반응물2-Chloro-6,7-dimethoxy-4-quinazolinamineHCID 90235—
반응물1-(Tetrahydro-2-furoyl)piperazineHCID 2734641—
용매EthanolHCID 702—
생성물Terazosin Hydrochloride AnhydrousHCID 4438393.1%

반응 조건

온도70 °C

반응 단계

A slurry of 60 grams (0.25 mol) of 4-amino-2-chloro-6,7-dimethoxy-quinazoline, 55.3 g (0.3 tool) of 1-(2-tetrahydrofuroyl)piperazine and 175 grams of 2-methoxyethanol was heated, under a nitrogen atmosphere with mechanical stirring, to 120°-123° C. for eight hours. The slurry was then cooled to 70° C. and 140 ml of 3A 200 proof ethanol was added. The resulting mixture was heated to 60°-70° C. for one hour and then cooled to 0°-5° C. To the cooled solution was added 2.5 g of concentrated aqueous hydrochloric acid in 12 ml of 3A 200 proof ethanol. This mixture was kept at -5°-5° C. for one and one-half hours after which the precipitated solid was collected by filtration and washed with 50 ml of cold 3A 200 proof ethanol to yield 98.7 g (0.233 tool, 93%) of anhydrous 1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-(2-tetrahydrofuroyl)piperazine hydrochloride of a previously unknown crystalline modification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05504207
출처 데이터셋uspto-grants-1996_04
ORD IDord-343667649537415faf00a186b0574759
출처 메모uspto-grants-1996_04