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4-(Bromomethyl)benzoic acid → 4-((1-Methylspiro[indolin-3,4'-piperidin]-1'-yl)methyl)benzoic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-(Bromomethyl)benzoic acid | HCID 22599 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 1-Methyl-1,2-dihydrospiro[indole-3,4'-piperidine] | HCID 10655739 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 4-((1-Methylspiro[indolin-3,4'-piperidin]-1'-yl)methyl)benzoic acid | HCID 70926855 | 142.5% |
反応手順
A mixed solution of 1-methylspiro[indolin-3,4′-piperidine] (1.0 g) synthesized according to a method described in [WO 2011/046851 pamphlet, (preparation 15)], 4-(bromomethyl)benzoic acid (1.08 g), and N,N-diisopropylethylamine (2.61 mL) in ethanol (20 mL) was heated and refluxed for 2 hours. To the resultant reaction mixture, N,N-diisopropylethylamine (1.04 mL) was further added, and the resultant reaction mixture was heated and refluxed for 2 hours. The reaction solution was left to reach room temperature, and from the reaction solution, the solvent was distilled off under reduced pressure to obtain a mixture (2.37 g) containing the subject compound. The resultant mixture was used in the next reaction without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08557766B2 |
| 出典データセット | uspto-grants-2013_10 |
| ORD ID | ord-461db4dc48d640459cb2cd64094927f0 |
| 出典メモ | uspto-grants-2013_10 |