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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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물P,P-Diphenylphosphinic azideHCID 199401—
반응물4-(5-Aminomethylfuran-2-yl)-2-(diaminomethyleneamino)thiazoleHCID 10399268—
반응물3-(Acetyloxy)propanoic acidHCID 12647151—
용매BenzeneHCID 241—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물4-[5-{3-(2-Acetoxyethyl)ureido}methylfuran-2-yl]-2-(diaminomethyleneamino)thiazoleHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05308857
출처 데이터셋uspto-grants-1994_05
ORD IDord-1e35ba9396e84701a89f6491da912058
출처 메모uspto-grants-1994_05