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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 85373생성일: 2026년 10월 25일

Imidazole → 2-hydroxy-N-(2-((4Z,7Z,10Z,13Z,16Z,19Z)-N-methyldocosa-4,7,10,13,16,19-hexaenamido)ethyl)benzamide

https://huagongshe.com/reaction/85373

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물Salicyloyl chlorideHCID 74041—
반응물(4Z,7Z,10Z,13Z,16Z,19Z)-N-(2-aminoethyl)-N-methyldocosa-4,7,10,13,16,19-hexaenamideHCID 59193341—
용매Ethyl AcetateHCID 8857—
생성물2-hydroxy-N-(2-((4Z,7Z,10Z,13Z,16Z,19Z)-N-methyldocosa-4,7,10,13,16,19-hexaenamido)ethyl)benzamideHCID 5919330173.4%

반응 단계

To a solution of (4Z,7Z,10Z,13Z,16Z,19Z)—N-(2-aminoethyl)-N-methyldocosa-4,7,10,13,16,19-hexaenamide (104 mg, 0.27 mmol), 2-hydroxybenzoyl chloride (37 mg, 0.27 mmol) and imidazole (19 mg, 0.27 mmol) in EtOAc (4 mL) at 0° C. was added dropwise a solution of DCC (0.57 g, 0.27 mmol) in EtOAc (4 mL). The mixture was stirred (RT, 16 h), filtered and concentrated under reduced pressure. The crude material was purified by chromatography on silica gel, eluting with EtOAc-PE (1:3) to afford 2-hydroxy-N-(2-((4Z,7Z,10Z,13Z,16Z,19Z)—N-methyldocosa-4,7,10,13,16,19-hexaenamido)-ethyl)-benzamide (100 mg, 73%) as a colorless oil. Mass calculated for C32H44N2O3=504.70; found: [M+H]+=505.5.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846972B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-92226bb7292b4619b13279511c88b3aa
출처 메모uspto-grants-2014_09