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HRID 1251생성일: 2026년 10월 24일

Triethylamine → 4-(2-Chlorophenyl)-2-(2-hydroxyimino-ethoxymethyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylic acid 3-ethyl 5-methyl ester

https://huagongshe.com/ko/reaction/1251

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Hydroxyammonium hydrochlorideHCID 22029257—
반응물4-(2-Chlorophenyl)-2-methyl-6-(2-oxo-ethoxymethyl)-1,4-dihydro-3,5-pyridinedicarboxylic acid 5-ethyl 3-methyl esterHCID 86752180—
용매MethanolHCID 887—
생성물4-(2-Chlorophenyl)-2-(2-hydroxyimino-ethoxymethyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylic acid 3-ethyl 5-methyl esterHCID 73078080—

반응 단계

A mixture of 4-(2-chlorophenyl)-2-methyl-6-(2-oxo-ethoxymethyl)-1,4-dihydro-3,5-pyridinedicarboxylic acid 5-ethyl 3-methyl ester (ID, 6.2 g), hydroxylammonium hydrochloride (1.27 g) and triethylamine (1.85 g) in methanol (100 mL) was stirred at room temperature for 6 h. Methanol was removed under reduced pressure and the residue was dissolved in ethyl acetate (200 mL) and water (200 mL). With vigorous stirring, the pH of the mixture was adjusted to 10 with aqueous 1N sodium hydroxide solution. After stirring for a further 15 min, the organic layer was collected, dried (sodium sulfate), filtered and concentrated in vacuo. The residue was recristallized from ether and hexane to give the title compound IB (6.1 g). HRMS: calc. for C20 H23CIN2O6 422.1245 found 422.1248; m.p. 161.4°-162.2° C.; IR (KBr, cm-1): 3446, 3379, 1698, 1671, 1601.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723618
출처 데이터셋uspto-grants-1998_03
ORD IDord-4264e1627523496cb0a0bc9ac274b94e
출처 메모uspto-grants-1998_03