돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 267082생성일: 2026년 10월 27일

Triethylamine → N-Methoxy-N-methyl-1-(2-naphthylmethyl)-1H-imidazol-5-ylacetamide

https://huagongshe.com/reaction/267082

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-hydroxy-1,2,3-benzotriazin-4(3H)-oneHCID 73026—
반응물Sodium BicarbonateHCID 516892—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-(2-naphthylmethyl)-1H-imidazol-5-ylacetic acid hydrochlorideHCID 70206205—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-Methoxy-N-methyl-1-(2-naphthylmethyl)-1H-imidazol-5-ylacetamideHCID 86751125—

반응 단계

To a solution of 1-(2-naphthylmethyl)-1H-imidazol-5-ylacetic acid hydrochloride (prepared in Example 4, 0.819 mg, 2.70 mmol) in dimethylformamide (15 ml) was added sequentially N, O-dimethylhydroxylamine hydrochloride (293 mg, 3.0 mmol), 3-hydroxy-1,2,3-benzotriazin-4(3H)-one (HOOBT, 489 mg, 3.0 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC, 575 mg, 3.0 mmol) and triethylamine (1.67 ml, 12.0 mmol) and the resulting mixture stirred at room temperature for 18 h. Saturated aq. sodium bicarbonate (30 ml) and water (30 ml) were added and the mixture was extracted with methylene chloride (2×50 ml). The combined organic extracts were washed with brine (50 ml) and the solvent evaporated in vacuo. The residue was purified by flash chromatography (2-4% methanol/methylene chloride gradient elution) to provide the title compound as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05652257
출처 데이터셋uspto-grants-1997_07
ORD IDord-b1467f2bd5694d53a51470721eae605e
출처 메모uspto-grants-1997_07