참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 2-Methoxyethanol | HCID 8019 | — |
| 반응물 | 2-Chloro-6,7-dimethoxy-4-quinazolinamine | HCID 90235 | — |
| 반응물 | 1-(Tetrahydro-2-furoyl)piperazine | HCID 2734641 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | Terazosin Hydrochloride Anhydrous | HCID 44383 | 93.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05504207 |
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| 출처 데이터셋 | uspto-grants-1996_04 |
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| ORD ID | ord-343667649537415faf00a186b0574759 |
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| 출처 메모 | uspto-grants-1996_04 |
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