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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1182152생성일: 2026년 10월 26일

Phenyl 5-ethyl-1,3,4-thiadiazol-2-ylcarbamate → 1-{3-[3-(4-Chloro-benzyl)-azetidin-1-yl]-propyl}-3-(5-ethyl-[1,3,4]thiadiazol-2-yl)-urea

https://huagongshe.com/reaction/1182152

반응식

참여 물질

역할이름HCID투입량
반응물Phenyl 5-ethyl-1,3,4-thiadiazol-2-ylcarbamateHCID 66876196—
반응물3-(3-(4-Chlorobenzyl)azetidin-1-yl)propan-1-amineHCID 69409123—
용매Dimethyl SulfoxideHCID 679—
생성물1-{3-[3-(4-Chloro-benzyl)-azetidin-1-yl]-propyl}-3-(5-ethyl-[1,3,4]thiadiazol-2-yl)-ureaHCID 10150676—

반응 단계

A solution of 3-[3-(4 chloro-benzyl)-azetidin-1-yl]-propylamine (0.100 mg, 0.418 mmol) and (5-ethyl-[1,3,4]thiadiazol-2-yl)-carbamic acid phenyl ester (0.11 mg, 0.439 mmol) in DMSO is stirred at room temperature for 18 hours then partitioned between ethylacetate and water. The organic phase is washed with brine and dried over magnesium sulphate and evaporated. The crude product is purified by flash silica chromatography using 5% methanol in DCM as eluent to afford 1-{3-[3-(4-chloro-benzyl)-azetidin-1-yl]-propyl}-3-(5-ethyl-[1,3,4]thiadiazol-2-yl)-urea. [M+H] 394.1

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07288537B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-ada1071260eb4f528c5b64d0239dc748
출처 메모uspto-grants-2007_10