참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Azepane | HCID 8119 | — |
| 반응물 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 반응물 | 1-[3-(1H-benzo[d]imidazol-2-yl)-4-chlorophenyl]piperidin-4-one | HCID 59568243 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-[5-(4-Azepan-1-yl-piperidin-1-yl)-2-chloro-phenyl]-1H-benzoimidazole | HCID 44124120 | 58% |
반응 단계
To a suspension of 1-[3-(1H-benzoimidazol-2-yl)-4-chloro-phenyl]-piperidin-4-one (0.10 g, 0.31 mmol) in dichloromethane (2 mL) was added azepane (0.05 mL, 0.46 mmol). After 30 min stirring at room temperature a drop of acetic acid was added, and after 1 h a further aliquot of azepane (0.05 mL, 0.46 mmol) was added, followed by sodium triacetoxyborohydride (NaB(OAc)3H) (0.10 g, 0.46 mmol). The reaction mixture was stirred at room temperature overnight, then the solvent was removed under reduced pressure, and the crude product dissolved in dichloromethane (10 mL). To the solution PS-isocyanate resin (PS-NCO) (Argonaut, loading 0.93 mmol/g) was added, then the mixture was shaken at room temperature overnight and filtered. The solvent was removed under reduced pressure to obtain a solid residue that was washed with EtOAc and Et2O then dried to give the desired product (0.07 g, 58%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08592463B2 |
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| 출처 데이터셋 | uspto-grants-2013_11 |
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| ORD ID | ord-c92a700be4a84b15b19ba1d6ccec95b2 |
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| 출처 메모 | uspto-grants-2013_11 |
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