Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1033073생성일: 2026년 10월 25일
Triethylamine → 4-[5-{3-(2-Acetoxyethyl)ureido}methylfuran-2-yl]-2-(diaminomethyleneamino)thiazole
https://huagongshe.com/reaction/1033073
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| 반응물 | 4-(5-Aminomethylfuran-2-yl)-2-(diaminomethyleneamino)thiazole | HCID 10399268 | — |
| 반응물 | 3-(Acetyloxy)propanoic acid | HCID 12647151 | — |
| 용매 | Benzene | HCID 241 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-[5-{3-(2-Acetoxyethyl)ureido}methylfuran-2-yl]-2-(diaminomethyleneamino)thiazole | HCID 10021797 | — |
반응 단계
A mixture of 3-acetoxypropionic acid (2.5 g), diphenylphosphorylazide (4.3 ml) and triethylamine (2.6 ml) in dry benzene (50 ml) was stirred for an hour at 75° to 80° C. To the mixture was added to a mixture of 4-(5-aminomethylfuran-2-yl)-2-(diaminomethyleneamino)thiazole (3.0 g) in a solution of tetrahydrofuran (45 ml) and methanol (45 ml) at ambient temperature, and the mixture was stirred for 2.5 hours at the same temperature. Evaporation of a solvent gave a residue, which was purified by column chromatography on silica gel eluting with a mixture of ethyl acetate and methanol (9:1, V/V). The eluted fractions containing the desired product were collected and evaporated in vacuo. The residue was recrystallized from a mixture of methanol, dioxane and isopropyl ether to give 4-[5-{3-(2-acetoxyethyl)ureido}methylfuran-2-yl]-2-(diaminomethyleneamino)thiazole (1.82 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05308857 |
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| 출처 데이터셋 | uspto-grants-1994_05 |
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| ORD ID | ord-1e35ba9396e84701a89f6491da912058 |
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| 출처 메모 | uspto-grants-1994_05 |
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