Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131552생성일: 2026년 10월 26일
4-Quinolinecarboxaldehyde → Ethyl 1,2,3,4-tetrahydro-6-(hydroxy-4-quinolinylmethyl)-3-methyl-1-(2-methylpropyl)-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxylate
https://huagongshe.com/reaction/131552
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Quinolinecarboxaldehyde | HCID 78072 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 반응물 | Ethyl 3-methyl-1-(2-methylpropyl)-2,4-dioxo-1,2,3,4-tetrahydro-thieno[2,3-d]pyrimidine-5-carboxylate | HCID 5282568 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Ethyl 1,2,3,4-tetrahydro-6-(hydroxy-4-quinolinylmethyl)-3-methyl-1-(2-methylpropyl)-2,4-dioxothieno[2,3-d]pyrimidine-5-carboxylate | HCID 5282569 | — |
반응 단계
A solution of lithium diisopropylamide (5.52 g) in anhydrous THF (80 ml) was added dropwise over 1 h to a stirred solution of the product of step c) (8.02 g) and 4-quinolinecarboxaldehyde (8.12 g) in anhydrous THF (80 ml) at −78° C. under nitrogen. The mixture was stirred for a further 1 hour at −78° C. then quenched with glacial acetic acid (10 ml), allowed to warm to room temperature, diluted with saturated sodium bicarbonate solution (100 ml) and extracted into ethyl acetate (2×100 ml). The combined extracts were dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography, eluting with 3:2 ethyl acetate/i-hexane, to give the sub-title compound as a white solid (7.35 g). MS(ESI) 468 {M+H]+. δ 1HCDCl3 0.85 (3H,d), 0.88 (3H,d), 1.43 (3H,t), 2.10-2.16 (1H,m), 3.38 (3H,s), 3.49 (1H,dd), 3.61 (1H, s,br), 3.71 (1H,dd), 4.48 (2H,quartet), 6.78 (1H,s), 7.52 (1H,t), 7.72 (1H,t), 7.83 (1H,d), 7.90 (1H,d), 8.17 (1H,d), 9.02 (1H,d)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07384950B2 |
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| 출처 데이터셋 | uspto-grants-2008_06 |
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| ORD ID | ord-be19efb468db49dab3ea2944cc2e8b92 |
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| 출처 메모 | uspto-grants-2008_06 |
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