Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 517554생성일: 2026년 10월 23일
1-Hydroxybenzotriazole → 5-(4-(3-Bromobenzyl)-5-methylthiazol-2-yl)-3-(4-(trifluoromethoxy)phenyl)-1,2,4-oxadiazole
https://huagongshe.com/ko/reaction/517554
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Hydroxybenzotriazole | HCID 75771 | — |
| 반응물 | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| 반응물 | 4-(Trifluoromethoxy)benzamidoxime | HCID 2733309 | — |
| 반응물 | Ethyl 4-(3-bromobenzyl)-5-methylthiazole-2-carboxylate | HCID 86711493 | — |
| 촉매 | Acetic Acid | HCID 176 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 5-(4-(3-Bromobenzyl)-5-methylthiazol-2-yl)-3-(4-(trifluoromethoxy)phenyl)-1,2,4-oxadiazole | HCID 86711495 | 68% |
반응 단계
A solution of ethyl 4-(3-bromobenzyl)-5-methylthiazole-2-carboxylate (0.06 mmol, crude from previous step), EDC.HCl (12 mg, 0.1 mmol) and HOBT (10 mg, 0.1 mmol) in DMF (0.4 mL) was stirred at RT for 30 min. N-hydroxy-4-(trifluoromethoxy)benzimidamide (15 mg, 0.07 mmol) was added and the reaction mixture was stirred for 1 h at RT. DMF (2 mL) was added to the mixture with 2 drops of AcOH. The mixture was subsequently heated to 140° C. for additional 2 h and then cooled to RT, diluted with H2O and taken into EtOAc. The organic layer was washed with NaHCO3, concentrated, and purified by silica gel column chromatography(0-45% EtOAc/Hexane) to give the titled compound (19 mg, 68%). MS (ES+) C20H13BrF3N3O2S requires: 495, 497, found: 496, 498 [M+H]+(1:1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09115120B2 |
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| 출처 데이터셋 | uspto-grants-2015_08 |
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| ORD ID | ord-a2786c6924934814a4cea2356ca0a92b |
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| 출처 메모 | uspto-grants-2015_08 |
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