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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 351824생성일: 2026년 10월 26일

Methylhydrazine → 3-cyclopropyl-[1,2,4]oxadiazol-5-ylmethyl-N,N-dimethyl-formamidine

https://huagongshe.com/reaction/351824

반응식

참여 물질

역할이름HCID투입량
반응물MethylhydrazineHCID 6061—
반응물N-PhthaloylglycineHCID 20825—
반응물N'-HydroxycyclopropanecarboximidamideHCID 2794666—
반응물4-(Aminomethyl)-3-cyclopropyl-1,2,4-oxadiazoleHCID 22713490—
반응물N-[(3-cyclopropyl-1,2,4-oxadiazol-5-yl)methyl]phthalimideHCID 22713498—
용매1,2-DichloroethaneHCID 11—
용매DimethylformamideHCID 6228—
용매1,1'-CarbonyldiimidazoleHCID 68263—
생성물3-cyclopropyl-[1,2,4]oxadiazol-5-ylmethyl-N,N-dimethyl-formamidineHCID 86585599—

반응 조건

온도130 °C

반응 단계

Scheme 3 describes the preparation of known starting materials. The processes for preparation of these compounds are also known or may be carried out in analogous manner to known methods. For example, N-[(3-cyclopropyl-1,2,4-oxadiazol-5-yl)methyl]phthalimide is prepared by reaction of N-phthaloylglycine in DMF and 1,1′carbonyldiimidazole, and followed by the addition of cyclopropanecarboxamidoxime. The obtained N-[(3-cyclopropyl-1,2,4-oxadiazol-5-yl)methyl]phthalimide is then dissolved in 1,2-dichloroethane and N-methylhydrazine is added. The obtained 4-(aminomethyl)-3-cyclopropyl-1,2,4-oxadiazole is then treated with N,N-dimethylformaldehyde diethyl acetal and heated at about 130° C. and the desired starting material (E/Z)-N′-(3-cyclopropyl-[1,2,4]oxadiazol-5-ylmethyl-N,N-dimethyl-formamidine is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06743789B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-72e9f2e9c5ca4a129d217bbf2e0400c1
출처 메모uspto-grants-2004_06