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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2039687생성일: 2026년 10월 27일

Pyridine → But-2-yn-1-yl {6-[({[(4-methyl-1,2,5-thiadiazol-3-yl)(phenyl)methylidene]-amino}oxy)methyl]pyridin-2-yl}carbamate

https://huagongshe.com/reaction/2039687

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물2-Butyn-1-yl chloroformateHCID 4131669—
반응물6-[[(Z)-[(4-methyl-1,2,5-thiadiazol-3-yl)-phenylmethylidene]amino]oxymethyl]pyridin-2-amineHCID 87394816—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매1,4-DioxaneHCID 31275—
생성물But-2-yn-1-yl {6-[({[(4-methyl-1,2,5-thiadiazol-3-yl)(phenyl)methylidene]-amino}oxy)methyl]pyridin-2-yl}carbamateHCID 8665983893%

반응 단계

To a stirred solution of 6-[({[(Z)-(4-methyl-1,2,5-thiadiazol-3-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-amine (100 mg, 0.31 mmol) in dry 1,4-dioxane (5 mL) were added pyridine (37 μL, 0.46 mmol) and but-2-yn-1-yl carbonochloridate (82 mg, 0.62 mmol). The reaction mixture was stirred at room temperature for 18 h, then diluted with DCM (10 mL) and water (10 mL), the organic layer was dried (MgSO4) and concentrated in vacuo. Purification on silica gel afforded but-2-yn-1-yl {6-[({[(4-methyl-1,2,5-thiadiazol-3-yl)(phenyl)methylidene]-amino}oxy)methyl]pyridin-2-yl}carbamate as a colourless oil [120 mg, yield 93%; HPLC/MS: m/z=422 (M+H); log P(HCOOH)=4.28].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08580799B2
출처 데이터셋uspto-grants-2013_11
ORD IDord-81e3130386c241c88baacb14db14e25c
출처 메모uspto-grants-2013_11