6825-71-4

基本信息
3,5-二氨基-1H-吡唑-4-羧酸乙酯
乙基3,5-二氨基-1H-吡唑-4-羧酸乙酯
EOS-61556
3,5-Diamino-4-ethoxycarbonylpyrazole
Ethyl 3,5-diamino-4-pyrazolecarboxylate
Ethyl 3,5-diamino-4-pyrazoxycarboxylic acid
ethyl 3,5-diaMino-1H-pyrazole-4-carboxylate
3,5-Diamino-1H-pyrazole-4-carboxylic acid ethyl ester
1H-Pyrazole-4-carboxylic acid, 3,5-diamino-, ethyl ester
物理化學(xué)性質(zhì)
制備方法

49765-05-1

6825-71-4
以(Z)-3-氨基-4,4,4-三氯-2-氰基丁-2-烯酸乙酯為原料合成3,5-二氨基-1H-吡唑-4-羧酸乙酯的一般步驟:將肼(2.19 mL,70 mmol)加入到(Z)-3-氨基-4,4,4-三氯-2-氰基丁-2-烯酸乙酯(15.0 g,58 mmol)的DMF(50 mL)溶液中。將反應(yīng)混合物加熱至100℃并保持1小時(shí),隨后冷卻至室溫。在真空條件下除去DMF,將殘余物在DCM與2M甲醇氨溶液的95:5(v/v)混合物中漿化。過(guò)濾收集所得沉淀,用95:5的DCM:MeOH混合物洗滌,并在真空下干燥,得到5.72 g(產(chǎn)率58%)的3,5-二氨基-1H-吡唑-4-羧酸乙酯,為白色固體。1H NMR(400 MHz,DMSO)δ 10.53(s,1H),5.28(br,4H),4.14(q,J = 7.1 Hz,2H),1.33-1.15(t,J = 7.1 Hz,3H)。
參考文獻(xiàn):
[1] Patent: WO2015/73267, 2015, A1. Location in patent: Paragraph 317; 367
[2] Patent: CN104650092, 2017, B. Location in patent: Paragraph 0463-0464; 0469-0470
[3] Patent: CN108003161, 2018, A. Location in patent: Paragraph 0849; 0855-0857
[4] Patent: WO2011/3065, 2011, A2. Location in patent: Page/Page column 110