Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29090생성일: 2026년 10월 23일
Ethyl Acetate → Methyl 4-(4-fluorophenyl)-2-isopropyl-8-methanesulfonyl-5,6,7,8-tetrahydro-[1,8]naphthyridine-3-carboxylate
https://huagongshe.com/ko/reaction/29090
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | 3,5-Dimethylpyridine | HCID 11565 | — |
| 반응물 | Methanesulfonic anhydride | HCID 81560 | — |
| 반응물 | Methyl 4-(4-fluorophenyl)-2-isopropyl-5,6,7,8-tetrahydro-[1,8]naphthyridine-3-carboxylate | HCID 11232707 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Methyl 4-(4-fluorophenyl)-2-isopropyl-8-methanesulfonyl-5,6,7,8-tetrahydro-[1,8]naphthyridine-3-carboxylate | HCID 11407102 | 86.1% |
반응 단계
A solution of (MeSO2)2O (15.9 g, 0.091 mol) in anhydrous CH2Cl2 (50 mL) was added to a solution of Part C methyl 4-(4-fluorophenyl)-2-isopropyl-5,6,7,8-tetrahydro-[1,8]naphthyridine-3-carboxylate (10. g, 0.030 mol) and 3,5-lutidine (20.9 mL, 0.182 mol) in anhydrous toluene (100 mL) at room temperature. The reaction mixture was stirred at room temperature for 3 days. Ethyl acetate (200 mL) and H2O (50 mL) were added, and the resulting two phases were separated. The organic phase was washed with aqueous NaHCO3 (5%, 50 mL), followed by half-saturated brine (50 mL). The solvent was removed under reduced pressure to afford a yellowish oil which solidified slowly. The crude material was recrystallized from i-PrOH/H2O (85:15, 45 mL) to afford 10.5 g (85% yield) of methyl 4-(4-fluorophenyl)-2-isopropyl-8-methanesulfonyl-5,6,7,8-tetrahydro-[1,8]naphthyridine-3-carboxylate as a off-white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07420059B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-f1e16f2f645848c08392fcd476819a3b |
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| 출처 메모 | uspto-grants-2008_09 |
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