Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 259644생성일: 2026년 10월 24일
Hexamethylphosphoramide → 2-(7-Methoxy-1,8-naphthyridin-2-yl)-3-(4-methylpiperazin-1-yl)carbonyloxy-isoindolin-1-one
https://huagongshe.com/ko/reaction/259644
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hexamethylphosphoramide | HCID 12679 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 4-Methyl-1-piperazinecarbonyl chloride | HCID 3016935 | — |
| 반응물 | 2-(7-Methoxy-1,8-naphthyridin-2-yl)-3-hydroxy-1-isoindolinone | HCID 14182181 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-(7-Methoxy-1,8-naphthyridin-2-yl)-3-(4-methylpiperazin-1-yl)carbonyloxy-isoindolin-1-one | HCID 21422109 | 45.9% |
반응 단계
Sodium hydride (50% dispersion in mineral oil) (0.8 g.) is added to a suspension of 2-(7-methoxy-1,8-naphthyridin-2-yl)-3-hydroxy-isoindolin-1-one (4.63 g.) in anhydrous dimethylformamide (45 cc.), whilst keeping the temperature between 18°-20° C. The reaction mixture is stirred for a further 4 hours 30 minutes. A solution of 1-chlorocarbonyl-4-methylpiperazine (2.7 g.) in anhydrous dimethylformamide (25 cc.) is then added over the course of 15 minutes and at a temperature of 20° C. The suspension is stirred for 17 hours at a temperature of about 20° C., and then anhydrous hexamethylphosphotriamide (7 cc.) is added. After 15 minutes, the reaction mixture is poured into ice-water (500 g.). The precipitate is filtered off and washed with water (45 cc.). A product (6.1 g.) is obtained and is recrystallised from diisopropyl ether (1,500 cc.). 2-(7-Methoxy-1,8-naphthyridin-2-yl)-3-(4 -methylpiperazin-1-yl)carbonyloxy-isoindolin-1-one (3 g.), melting at 191° C., is thus obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04038391 |
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| 출처 데이터셋 | uspto-grants-1977_07 |
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| ORD ID | ord-f6d9a6c5b14e4618a54b3b7e9798e706 |
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| 출처 메모 | uspto-grants-1977_07 |
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