化工社化工社 化学情報印刷レポート · 研究参考用
2-Chloro-6,7-dimethoxy-4-quinazolinamine → Terazosin Hydrochloride Anhydrous
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Chloro-6,7-dimethoxy-4-quinazolinamine | HCID 90235 | — |
| 反応物 | 1-(Tetrahydro-2-furoyl)piperazine | HCID 2734641 | — |
| 溶媒 | 1-Methoxyethanol | HCID 3015637 | — |
| 生成物 | Terazosin Hydrochloride Anhydrous | HCID 44383 | — |
反応手順
To 7.00 g 2-chloro-4-amino-6,7-dimethoxyquinazoline (Lancaster Synthesis) in 50 ml methoxyethanol was added 10.8 g, tetrahydrofuroylpiperazine, and the mixture refluxed 3 hours. The clear solution was concentrated and an aqueous solution of potassium bicarbonate was added. The resultant solid that formed was filtered and washed with water. It was then added to methanol and the resulting suspension was acidified with a solution of hydrogen chloride in isopropyl alcohol. The resulting solution was concentrated and the residue crystallized from isopropyl alcohol giving 8.12 g. of product, m.p. 278°-279° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05403847 |
| 出典データセット | uspto-grants-1995_04 |
| ORD ID | ord-0e41a6faa1c04f1c9c0eadce49ddc28e |
| 出典メモ | uspto-grants-1995_04 |