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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 963028생성일: 2026년 10월 25일

Citric Acid → N-(4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl)-5-methyl[1,2,4]triazol-3-ylmethyl)naphthalene-2-caboxamide

https://huagongshe.com/reaction/963028

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물2-Naphthoic acidHCID 7123—
반응물P,P-Diphenylphosphinic azideHCID 199401—
반응물3-Aminomethyl-4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl)-5-methyl[1,2,4]triazole ditosylateHCID 19085095—
용매DimethylformamideHCID 6228—
용매TriethylamineHCID 8471—
생성물N-(4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl)-5-methyl[1,2,4]triazol-3-ylmethyl)naphthalene-2-caboxamideHCID 6766455319.6%

반응 단계

3-Aminomethyl-4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl)-5-methyl[1,2,4]triazole di-p-toluenesulfonate (3.70 g) was dissolved in dimethylformamide (20 ml). Naphthalene-2-carboxylic acid (0.95 g) and diphenylphosphoryl azide (1.29 ml) were added under ice-cooling and dissolved in the solution. A solution of triethylamine (2.24 ml) in dimethylformamide was dropwise added, and the mixture was allowed to stand overnight at room temperature. Then, a 10% aqueous citric acid solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium hydrogencarbonate solution and saturated brine, and dried over magnesium sulfate. The solvent was evaporated, and the residue was recrystallized from ethyl acetate to give 0.53 g of N-(4-(3-(2-chlorobenzoyl)-5-ethylthiophen-2-yl)-5-methyl[1,2,4]triazol-3-ylmethyl)naphthalene-2-caboxamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05760032
출처 데이터셋uspto-grants-1998_06
ORD IDord-e92a2836da4e46778b935b1390037bab
출처 메모uspto-grants-1998_06