Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4851생성일: 2026년 10월 25일
Potassium Carbonate → (E)-but-2-enedioic acid;4-methyl-2-[2-(2-methylpyrrolidin-1-yl)ethyl]-2,3-dihydropyrido[3,2-f][1,4]oxazepine-5-thione;propan-2-ol
https://huagongshe.com/reaction/4851
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2-Methylpyrrolidine | HCID 13003 | — |
| 반응물 | Fumaric Acid | HCID 444972 | — |
| 반응물 | 2-(chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f]-1,4-oxazepine-5(4H)thione | HCID 13726442 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | (E)-but-2-enedioic acid;4-methyl-2-[2-(2-methylpyrrolidin-1-yl)ethyl]-2,3-dihydropyrido[3,2-f][1,4]oxazepine-5-thione;propan-2-ol | HCID 14391511 | 32.8% |
반응 단계
To a suspension of 5.0 g (0.019 mole) of 2-(chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f]-1,4-oxazepine-5(4H)-thione in 25 ml of absolute ethanol was added 3.5 g (0.04 mole) of 2-methylpyrrolidine. The mixture was heated to reflux for 6.5 hr and left standing at room temperature overnight. Mass spec and TLC showed presence of starting materials. Approximately 5 g of potassium carbonate was added and heating at reflux was continued for 24 hr. Ethanol was removed by rotary evaporation (70° C., 30 mm). The residue was taken up in 100 ml of methylene chloride and washed with 2×50 ml dil. aqueous sodium hydroxide. The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation (70° C., 30 mm). The residual syrup was dissolved in isopropyl aocohol and treated with fumaric acid affording 4.5 g (0.01 mole, 49.2%) of crude crystals. Two recrystallizations from isopropyl afforded 1.5 g (16.4%) of yellow crystals, m.p., 92°-95° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04727152 |
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| 출처 데이터셋 | uspto-grants-1988_02 |
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| ORD ID | ord-f80487ff4d8a47d2b5d758272f0f2d59 |
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| 출처 메모 | uspto-grants-1988_02 |
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