1053656-57-7

基本信息
tert-Butyl 4-chloro-5H,6H,8H-pyrido[3,4-d]pyrimidine-7-carboxylate
tert-butyl 4-chloro-6,8-dihydro-5H-pyrido[3,4-d]pyrimidine-7-carboxylate
4-chloro-5,8-dihydro-6H-pyrido[3,4-d]pyriMidine-7-carboxylic acid tert-butyl ester
Pyrido[3,4-d]pyrimidine-7(6H)-carboxylic acid, 4-chloro-5,8-dihydro-, 1,1-dimethylethyl ester
物理化学性质
制备方法
![4-氧代-3,4,5,6-四氢吡啶并[3,4-d]吡啶-7(8H)-甲酸叔丁酯](/CAS/GIF/1142188-60-0.gif)
1142188-60-0
![4-氯-5,6-二氢吡咯并[3,2-D]吡啶-7-甲酸叔丁酯](/CAS/20180808/GIF/1053656-57-7.gif)
1053656-57-7
以4-羟基-5,6-二氢吡啶并[3,4-d]嘧啶-7(8H)-羧酸叔丁酯为原料合成4-氯-5,8-二氢吡啶并[3,4-d]嘧啶-7(8H)-甲酸叔丁酯的一般步骤:向中间体1(1.26g,5.02mmol)在二氯乙烷(DCE,36mL)中的溶液中依次加入三苯基膦(PPh3,2.69g,10.05mmol)和四氯化碳(CCl4,1.46mL,15.07mmol)。将反应混合物加热至70℃,维持2.5小时。反应完成后,将混合物在减压下浓缩,通过硅胶(SiO2)柱色谱进行纯化,以乙酸乙酯/己烷为洗脱剂,得到目标化合物为浅黄色固体(1.20g,收率88%)。质谱(ESI)计算值C12H16ClN3O2为269.09,实测值m/z 270.1 [M + H]+。1H NMR(400MHz,CDCl3)δ:8.79(s,1H),4.65(br s,2H),3.80-3.68(m,2H),2.93-2.82(m,2H),1.49(s,9H)。
参考文献:
[1] Patent: US2014/275120, 2014, A1. Location in patent: Paragraph 0160; 0161
[2] Patent: WO2011/29842, 2011, A1. Location in patent: Page/Page column 40-41
[3] ACS Medicinal Chemistry Letters, 2013, vol. 4, # 2, p. 186 - 190
[4] Patent: US2016/75708, 2016, A1. Location in patent: Paragraph 0086; 0092
[5] Patent: KR2015/139962, 2015, A. Location in patent: Paragraph 0118-0119; 0131-0132