101667-98-5
101667-98-5 結(jié)構(gòu)式
基本信息
4-氯-5-甲基噻吩并[2,3-D]嘧啶-6-甲酸乙酯
4-Chloro-5-methylthieno[2,3-d]pyrimidine-6-carboxylic acid ethyl ester
Thieno[2,3-d]pyrimidine-6-carboxylic acid, 4-chloro-5-methyl-, ethyl ester
物理化學(xué)性質(zhì)
制備方法
17417-67-3
101667-98-5
以5-甲基-4-氧代-3,4-二氫噻吩并[2,3-D]-嘧啶-6-羧酸乙酯(425mg,1.783mmol)為原料,在甲苯(8mL)中溶解后,依次加入N,N-二異丙基乙胺(DIPEA,248μL,1.426mmol,0.8當(dāng)量)和三氯氧磷(POCl3,199μL,2.14mmol,1.2當(dāng)量)。將反應(yīng)混合物置于120-125℃油浴中加熱回流3小時(shí)。反應(yīng)完成后,將混合物冷卻至室溫,隨后緩慢倒入冰冷卻的飽和碳酸氫鈉水溶液(20mL)和乙酸乙酯(EtOAc,50mL)的混合體系中,并迅速攪拌以徹底淬滅過量的三氯氧磷。分離有機(jī)相和水相,有機(jī)相再用飽和碳酸氫鈉水溶液(20mL)洗滌一次。有機(jī)層經(jīng)無水硫酸鈉(Na2SO4)干燥后,過濾并減壓濃縮,得到4-氯-5-甲基噻吩并[2,3-d]嘧啶-6-羧酸乙酯(25B)為黃色固體(432mg,收率94%)。
參考文獻(xiàn):
[1] Patent: WO2005/42537, 2005, A1. Location in patent: Page/Page column 57
[2] European Journal of Medicinal Chemistry, 2016, vol. 115, p. 148 - 160
[3] Bioorganic and Medicinal Chemistry Letters, 2018, vol. 28, # 9, p. 1663 - 1669
[4] Pharmazie, 1993, vol. 48, # 3, p. 192 - 194
[5] Chemistry of Heterocyclic Compounds (New York, NY, United States), 1985, vol. 21, # 7, p. 767 - 770