158406-99-6

基本信息
(S)-3-(溴甲基)哌啶-1-羧酸叔丁酯
叔-丁基 (3S)-3-(溴甲基)哌啶-1-甲酸基酯
tert-butyl (3S)-3-(bromomethyl)piperidine-1-carboxylate
(S)-tert-Butyl 3-(bromomethyl)piperidine-1-carboxylate
(S)-3-Bromomethyl-piperidine-1-carboxylic acid tert-butyl ester
1-Piperidinecarboxylic acid, 3-(bromomethyl)-, 1,1-dimethylethyl ester, (3S)-
物理化學(xué)性質(zhì)
制備方法

140695-84-7

158406-99-6
以(S)-3-(羥甲基)哌啶-1-羧酸叔丁酯為原料合成(S)-3-(溴甲基)哌啶-1-羧酸叔丁酯的一般步驟:將(S)-3-(羥甲基)哌啶-1-羧酸叔丁酯(30.0g,139mmol)和四溴化碳(72.0g,217mmol)溶解于二氯甲烷(150mL)中。在冰浴冷卻下,保持反應(yīng)體系內(nèi)部溫度在20至25℃之間,緩慢滴加三苯基膦(42.4g,162mmol)的二氯甲烷(150mL)溶液。滴加完畢后,于室溫下繼續(xù)攪拌反應(yīng)混合物1小時。隨后,加入環(huán)己烷(500mL),并在減壓條件下蒸發(fā)除去約一半的溶劑。將剩余溶液置于冰浴中冷卻,過濾除去生成的沉淀。濾液經(jīng)減壓濃縮后,所得殘余物通過快速柱色譜法純化(洗脫劑:0至25%乙酸乙酯/己烷,硅膠為固定相),得到35.1g(產(chǎn)率91%)的(S)-3-(溴甲基)哌啶-1-羧酸叔丁酯,為固體。質(zhì)譜(電噴霧正離子模式)m/z 278([M+H]+)。
參考文獻(xiàn):
[1] Patent: WO2007/58850, 2007, A2. Location in patent: Page/Page column 41
[2] Journal of Medicinal Chemistry, 2008, vol. 51, # 18, p. 5663 - 5679
[3] Patent: WO2008/121685, 2008, A1. Location in patent: Page/Page column 38
[4] Patent: US2008/176901, 2008, A1. Location in patent: Page/Page column 9-10