Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127274생성일: 2026년 10월 26일
Sodium Carbonate → 8-[1-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-4-piperidinyl]-8-azaspiro[4,5]decan-7,9-dione hydrochloride
https://huagongshe.com/reaction/127274
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | 2-Chloro-6,7-dimethoxy-4-quinazolinamine | HCID 90235 | — |
| 반응물 | 8-(4-Piperidinyl)-8-azaspiro[4,5]decan-7,9-dione | HCID 12822553 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 8-[1-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-4-piperidinyl]-8-azaspiro[4,5]decan-7,9-dione hydrochloride | HCID 20556259 | — |
반응 단계
The mixture of 70 g of 4-amino-2-chloro-6,7-dimethoxyquinazoline, 73.2 g of 8-(4-piperidinyl)-8-azaspiro[4,5]decan-7,9-dione, 62.1 g of anhydrous sodium carbonate and 800 ml of dimethylformamide is stirred under nitrogen at 135° for 8 hours. It is allowed to cool to room temperature, filtered and the filtrate evaporated. The residue is poured with stirring and cooling into 300 ml of water, the mixture diluted with 1400 ml of water and filtered. The solids are triturated with 1600 ml of ethyl acetate and 10 ml of saturated aqueous sodium carbonate. The organic layer is separated, dried, evaporated and the residue dissolved in 1,000 ml of ethyl acetate. The solution is acidified with hydrogen chloride, the precipitate filtered off and recrystallized from aqueous methanol, to yield the 8-[1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-piperidinyl]-8-azaspiro[4,5]decan-7,9-dione hydrochloride melting at 277°-279° (dec.).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04255429 |
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| 출처 데이터셋 | uspto-grants-1981_03 |
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| ORD ID | ord-817b4e461ae54bd5af134e56c97373d5 |
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| 출처 메모 | uspto-grants-1981_03 |
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