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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 891051생성일: 2026년 10월 26일

3-(4-Tert-butylphenyl)-5-(chloromethyl)-1,2,4-oxadiazole → (2S)-3-[4-({3-[4-(tert-butyl)phenyl](1,2,4-oxadiazol-5-yl)}methyl)piperazinyl]-1-(2-methylbenzothiazol-5-yloxy)propan-2-ol

https://huagongshe.com/reaction/891051

반응식

참여 물질

역할이름HCID투입량
반응물3-(4-Tert-butylphenyl)-5-(chloromethyl)-1,2,4-oxadiazoleHCID 2781701—
반응물(2S)-1-(2-methylbenzothiazol-5-yloxy)-3-piperazinylpropan-2-olHCID 58595334—
용매Trimethylamine ethanolHCID 86589564—
생성물(2S)-3-[4-({3-[4-(tert-butyl)phenyl](1,2,4-oxadiazol-5-yl)}methyl)piperazinyl]-1-(2-methylbenzothiazol-5-yloxy)propan-2-olHCID 23598931—

반응 단계

A solution of (2S)-1-(2-methylbenzothiazol-5-yloxy)-3-piperazinylpropan-2-ol, a compound of formula (6) (75 mg, 0.14 mmol), and 3-(4-tert-butylphenyl)-5-chloromethyl-1,2,4-oxadiazole (40 mg, 0.16 mmol) in 10% trimethylamine/ethanol, was heated to 73° C. and allowed to stir overnight. The solvent was evaporated under reduced pressure, and the resulting residue chromatographed by PTLC (3% methanol/methylene chloride). The resulting oil was diluted with methylene chloride and placed on the high Vac. overnight, to yield (2S)-3-[4-({3-[4-(tert-butyl)phenyl](1,2,4-oxadiazol-5-yl)}methyl)piperazinyl]-1-(2-methylbenzothiazol-5-yloxy)propan-2-ol as a white solid (52 mg, 0.09 mmol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07001909B2
출처 데이터셋uspto-grants-2006_02
ORD IDord-9cf47494fad346a0bd0c93ea433dbbe1
출처 메모uspto-grants-2006_02