Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 634732생성일: 2026년 10월 25일
Hydrochloric Acid → 4-(2-Fluoro-5-hydroxy-4-methylanilino)-7-(3-morpholinopropionamido)quinazoline
https://huagongshe.com/reaction/634732
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 4-(2-Fluoro-5-methoxycarbonyloxy-4-methylanilino)-7-(3-morpholinopropionamido)quinazoline | HCID 21260355 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4-(2-Fluoro-5-hydroxy-4-methylanilino)-7-(3-morpholinopropionamido)quinazoline | HCID 21260319 | 80% |
반응 단계
2M Aqueous sodium hydroxide solution (453 μl, 0.9 mmol) was added to a suspension of 4-(2-fluoro-5-methoxycarbonyloxy-4-methylanilino)-7-(3-morpholinopropionamido)quinazoline (219 mg, 0.45 mmol) in methanol (6 ml) and the mixture stirred for 1 hour. The reaction mixture was diluted with water and then adjusted to pH6 with 2M hydrochloric acid. The resulting precipitate was collected by filtration, washed with water and ethanol, and dried. The solid was dissolved in methylene chloride/methanol and a 5M solution of hydrogen chloride in isopropanol (0.3 ml) added. The volatiles were removed by evaporation, the resulting solid was washed with ether, and dried under vacuum to give 4-(2-fluoro-5-hydroxy-4-methylanilino)-7-(3-morpholinopropionamido)quinazoline (1-86 mg, 80%) as a yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06184225B2 |
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| 출처 데이터셋 | uspto-grants-2001_02 |
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| ORD ID | ord-acf00f39016b4701a3e228fcd490f95f |
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| 출처 메모 | uspto-grants-2001_02 |
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