Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1967740생성일: 2026년 10월 25일
Dimethylformamide → 1-(Benzyloxycarbonyl)-N-[4-(2-furyl)-5-morpholinothiazol-2-yl]piperidine-4-carboxamide
https://huagongshe.com/reaction/1967740
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | 1-Carbobenzoxy-4-piperidinecarboxylic Acid | HCID 736489 | — |
| 반응물 | 2-Amino-4-(2-furyl)-5-morpholinothiazole | HCID 23144158 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 1-(Benzyloxycarbonyl)-N-[4-(2-furyl)-5-morpholinothiazol-2-yl]piperidine-4-carboxamide | HCID 23144107 | 100% |
반응 단계
1-Benzyloxycarbonylpiperidine-4-carboxylic acid (5.00 g, 19.0 mmol) was dissolved in dichloromethane (80 mL), and thionyl chloride (6.93 mL, 95.0 mmol) and DMF (0.15 mL, 1.90 mmol) were added thereto, followed by 178, stirring under heating and reflux for 3 hours. The reaction mixture was concentrated under reduced pressure, and the resulting residue was dissolved in dichloromethane (2 mL). The resulting solution was added to a solution of 2-amino-4-(2-furyl)-5-morpholinotliiazole (2.01 g, 8.00 mmol) in pyridine (32 mL) obtained in Step 1 of Example 29, and then N,N-dimethylaminopyridine (97.6 mg, 0.800 mmol) was added thereto, followed by stirring at room temperature for 1 hour. The solvent was distilled away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (hexane:ethyl acetate=1:1 to 1:3) to afford the entitled Compound 43 (4.96 g, 100%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08420827B2 |
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| 출처 데이터셋 | uspto-grants-2013_04 |
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| ORD ID | ord-ebe9cf2876e14ed9b289f4f371ed1393 |
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| 출처 메모 | uspto-grants-2013_04 |
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