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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5398생성일: 2026년 10월 24일

4-Methylmorpholine → 3-(N-[[trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecan-10-yl]-carbonyl]-amino)-pyridine

https://huagongshe.com/ko/reaction/5398

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물3-AminopyridineHCID 10009—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물trans 3-(Acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxylic acidHCID 86747202—
용매DichloromethaneHCID 6344—
생성물3-(N-[[trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecan-10-yl]-carbonyl]-amino)-pyridineHCID 86747206—

반응 조건

온도0 °C

반응 단계

Trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxylic acid (0.100 g, 0.35 mmol), 3-aminopyridine (0.036 g, 0.38 mmol), 1-hydroxybenzotriazole (0.047 g, 0.035 mmol), and 4-methylmorpholine (0.077 mL, 0.70 mmol) are dissolved in methylene chloride (2.5 mL), and the reaction is cooled to 0° C. To this solution is added N-(dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (0.134 g, 0.70 mmol), and the reaction is allowed to warm up to room temperature and then stirred overnight. The reaction is partitioned between methylene chloride and water, the organic layer is dried (MgSO4), and the solvent is evaporated. The product is purified by silica gel chromatography (70% ethyl acetate/hexane) to give 3-{N-[[trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecan-10-yl]-carbonyl]-amino}-pyridine, MS: M+1=364.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05244889
출처 데이터셋uspto-grants-1993_09
ORD IDord-37b24b9090dc4d9a9382a6652abf7b0e
출처 메모uspto-grants-1993_09