114457-94-2

基本信息
硼替佐米-B
硼替佐米中二
硼替佐米中間體
硼替佐米雜質(zhì)B
硼替佐米雜質(zhì)36
硼替佐米中間體2
硼替佐米中間體B
硼替佐米中間體二
1硼替佐米雜質(zhì)D
Bortezomib INT
Bortezomib INT B
Bortezomib impurity B
N-(2-pyrazinylcarbonyl)-
Bortezomib Acid Impurity
Bortezomib Intermediate 2
Bortezomib USP Impurity D
(S)-3-Phenyl-2-(pyrazine-2-carbox
N-Pyrazinylcarbonyl-L-phenylalanine
物理化學(xué)性質(zhì)
制備方法

73058-37-4

114457-94-2
以(吡嗪-2-羰基)-L-苯丙氨酸甲酯為原料合成(S)-3-苯基-2-(吡嗪-2-甲酰胺基)丙酸的一般步驟:將N-吡嗪甲酰基-L-苯丙氨酸甲酯(1.0g,3.51mmol)溶解于10mL丙酮中,在冰水浴冷卻下緩慢滴加2N NaOH溶液,調(diào)節(jié)pH至12~13。反應(yīng)過程中通過薄層色譜(TLC)監(jiān)測反應(yīng)進度,2小時后反應(yīng)完成。隨后,在冰水浴條件下緩慢滴加鹽酸,調(diào)節(jié)pH至2~3,此時有大量白色固體析出。過濾收集沉淀,依次用水和乙醚洗滌,然后于空氣中干燥。最終得到0.89g白色固體產(chǎn)物,產(chǎn)率為93.6%,熔點為166-169℃。產(chǎn)物結(jié)構(gòu)經(jīng)1H-NMR(DMSO-d6, 300MHz)確認:δ 3.23(-CH2,m,2H),4.74(-CH,m,1H),7.16~7.25(-Ph,m,5H),8.74(-CONH,t,1H),8.86~8.89(-Pyz,t,2H),9.14(-Pyz,d,1H),13.06(-COOH,s,1H)。
參考文獻:
[1] Patent: EP2444411, 2016, B1. Location in patent: Paragraph 0038
[2] Bioorganic and Medicinal Chemistry, 2017, vol. 25, # 15, p. 4031 - 4044
[3] Organic and Biomolecular Chemistry, 2007, vol. 5, # 9, p. 1416 - 1426
[4] Bioorganic and Medicinal Chemistry, 2009, vol. 17, # 19, p. 6851 - 6861
[5] Journal of Medicinal Chemistry, 2009, vol. 52, # 14, p. 4192 - 4199