Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1827880생성일: 2026년 10월 27일
Triethylamine → 3-(4-{[5-(3-Fluorophenyl)(1,2,4-oxadiazol-3-yl)]methyl}piperazinyl)-1-(2-methylbenzothiazol-5-yloxy)propan-2-ol
https://huagongshe.com/reaction/1827880
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 3-(Chloromethyl)-5-(3-fluorophenyl)-1,2,4-oxadiazole | HCID 10262618 | — |
| 반응물 | (2S)-1-(2-methylbenzothiazol-5-yloxy)-3-piperazinylpropan-2-ol | HCID 58595334 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 3-(4-{[5-(3-Fluorophenyl)(1,2,4-oxadiazol-3-yl)]methyl}piperazinyl)-1-(2-methylbenzothiazol-5-yloxy)propan-2-ol | HCID 22064288 | — |
반응 단계
3-(Chloromethyl)-5-(3-fluorophenyl)-1,2,4-oxadiazole (242 mg, 1.02 mmol) and (2S)-1-(2-methylbenzothiazol-5-yloxy)-3-piperazine-1-yl-propan-2-ol, a compound of formula (6) (309 mg, 1.0 mmol) in EtOH (8 mL) were treated with Et3N (0.5 mL, 3.57 mmol) and refluxed at 90° C. on a J-Kem™ block for 48 hours. The reaction product was concentrated and the product purified by flash chromatography (90:10 EtOAc-MeOH) to yield 3-(4-{[5-(3-fluorophenyl)(1,2,4-oxadiazol-3-yl)]methyl}piperazinyl)-1-(2-methylbenzothiazol-5-yloxy)propan-2-ol, a compound of Formula I.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07056924B2 |
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| 출처 데이터셋 | uspto-grants-2006_06 |
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| ORD ID | ord-d022231a58ee48089fa0cccd4c19e824 |
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| 출처 메모 | uspto-grants-2006_06 |
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