Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64635생성일: 2026년 10월 23일
Ethyl 2-methylacetoacetate → 6,7-dimethyl-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, methyl ester
https://huagongshe.com/ko/reaction/64635
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Ethyl 2-methylacetoacetate | HCID 701 | — |
| 반응물 | Methyl 2-aminothiazole-5-carboxylate | HCID 238005 | — |
| 생성물 | 6,7-dimethyl-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, methyl ester | HCID 15590861 | — |
반응 단계
2-amino-thiazole-5-carboxylic acid, methyl ester (5 g) was reacted with ethyl 2-methyl-acetoacetate (9.11 g) in polyphosphoric acid (25 g: 13.3 g of H3PO4 and 11.7 g of P2O5) under stirring at 100° C. for three hours. After cooling, dilution with ice water and neutralization with 20% NaOH, the precipitate was filtered, washed with water and crystallized from CH2Cl2 -hexane to give 6,7-dimethyl-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, methyl ester, m.p. 158°-159° C. (5.46 g), which was reacted with benzaldehyde (3.52 g) in methanol (120 ml) in the presence of sodium methylate (2.7 g) under stirring at reflux temperature for 120 hours. After cooling and concentration in vacuo, the precipitate was filtered and dissolved in a mixture of dimethylformamide and formic acid. The solution was diluted with ice water and the precipitate was filtered, washed with water until neutral and crystallized from isopropyl alcohol to give 2.8 g of 6-methyl-7-trans-(2-phenylethenyl)-5-oxo-5H-thiazolo[3,2-a]pyrimidine-2-carboxylic acid, m.p. 257°-259° C., N.M.R. (CF3COOD) δp.p.m.: 2.50 (s) (3H, --CH3), 7.36 (d) (1H, β-ethenyl proton), 7.40-7.90 (m) (5H, phenyl protons), 7.73 (d) (1H, α-ethenyl proton), 9.07 (s) (1H, C-3 proton), JHαHβ =16 Hz.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04609660 |
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| 출처 데이터셋 | uspto-grants-1986_09 |
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| ORD ID | ord-e205deed67764f13b40fba1ddc88bdfd |
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| 출처 메모 | uspto-grants-1986_09 |
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