Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1244379생성일: 2026년 10월 27일
Boron trifluoride etherate → 5-benzyl-2-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine
https://huagongshe.com/reaction/1244379
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Boron trifluoride etherate | HCID 8000 | — |
| 반응물 | 1-Benzyl-4,4-diethoxypiperidin-3-amine | HCID 21729935 | — |
| 반응물 | 4-Methoxy-7-morpholin-4-yl-benzothiazole-2-carboximidothioic acid methyl ester hydroiodide | HCID 69184072 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-benzyl-2-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine | HCID 21919258 | 1% |
반응 단계
To a suspension of 0.04 g 4-methoxy-7-morpholin-4-yl-benzothiazole-2-carboximidothioic acid methyl ester hydroiodide in 1.8 ml tetrahydrofurane were added 0.1 g 1-benzyl-4,4-diethoxy-piperidin-3-ylamine in 1.8 ml tetrahydrofurane and the mixture was stirred at room temperature for 16 hours. Then 0.015 ml boron trifluoride etherate was added and the solvent was distilled off under vacuum. Again 0.015 ml boron trifluoride etherate was added and the mixture was dissolved in 1.5 ml dimethylformamide and heated for 15 minutes at 125° C. The solvent was distilled off and the residue was dissolved in dichloromethane and extracted with water. The organic layer was dried with sodium sulfate, filtered and the solvent was evaporated. Chromatography on silicagel with ethylacatate/heptane 1:1 to 2:1 yielded 0.4 mg (1%) 5-benzyl-2-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine as an amorphous solid; m/e=462 (M+H+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07122545B2 |
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| 출처 데이터셋 | uspto-grants-2006_10 |
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| ORD ID | ord-11fac07d95c64a1cb1b38980ef5e47fc |
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| 출처 메모 | uspto-grants-2006_10 |
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