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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1914608생성일: 2026년 10월 26일

Triethylamine → N-{6-[({[(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}hex-5-ynamide

https://huagongshe.com/reaction/1914608

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Hex-5-ynoyl chlorideHCID 2759284—
반응물6-[({[(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-amineHCID 76832220—
용매DichloromethaneHCID 6344—
생성물N-{6-[({[(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}hex-5-ynamideHCID 8665656995%

반응 단계

To a solution of 6-[({[(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-amine (251 mg, 0.81 mmol) in dichloromethane (10 mL) was added triethylamine (0.22 mL, 1.62 mmol), hex-5-ynoyl chloride (211 mg, 1.62 mmol). The reaction mixture was stirred for 5 hours at room temperature, concentrated in vacuo, and then purified by silica gel chromatography to yield to N-{6-[({[(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}hex-5-ynamide [200 mg; 95% of purity; 58% of theory; HPLC/MS: m/z=404 (M+H); log P(HCOOH)=2.98].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08614217B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-3c88f41a314d40ac9e6eb223c5d6b951
출처 메모uspto-grants-2013_12