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tert-Butyl 4-formylpiperidine-1-carboxylate → tert-butyl {4-[1-butyl-4,6-di(3-diethylaminopropoxy)-1H-benzimidazol-2-yl]}piperidine-1-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | tert-Butyl 4-formylpiperidine-1-carboxylate | HCID 1514430 | — |
| 反応物 | 2-Butylamino-4,6-di(3-diethylaminopropoxy)aniline | HCID 66977544 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | tert-butyl {4-[1-butyl-4,6-di(3-diethylaminopropoxy)-1H-benzimidazol-2-yl]}piperidine-1-carboxylate | HCID 66977506 | 69% |
反応手順
A solution of 1-(t-butyloxycarbonyl)piperdine-4-carboxaldehyde (235 mg; 1.1 mmol) and 2-butylamino-4,6-di(3-diethylaminopropoxy)aniline (synthesized via General Procedures J1 and J2 and I) (424 mg; 1 mmol) in ethanol (5 mL) was subjected to General Procedure K. The crude product was purified by silica gel column chromatography using 10% MeOH in DCM with a gradual increment of triethylamine (0.2 to 1.0%) as eluent to afford 425 mg of tert-butyl {4-[1-butyl-4,6-di(3-diethylaminopropoxy)-1H-benzimidazol-2-yl]}piperidine-1-carboxylate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07737285B2 |
| 出典データセット | uspto-grants-2010_06 |
| ORD ID | ord-64ef82b016524b0e990e1594c8b1277f |
| 出典メモ | uspto-grants-2010_06 |