43120-28-1

基本信息
3-吲唑羧酸甲酯
吲唑-3-甲酸甲酯
1H-吲唑-3-甲酸甲酯
1H-吲唑-3-羧酸甲酯
1氫-吲唑-3-羧酸甲酯
1氫-吲唑-3-甲酸甲酯
甲基 1H-吲唑-3-甲酸基酯
1H-吲唑-3-羧酸甲酯(CAS號(hào):43120-28-1)
Methyl 1H-indazole-3-carb...
methyl indazole-3-carboxylate
METHYL INDAZOLYL-3-CARBOXYLATE
METHYL 1H-INDAZOLE-3-CARBOXYLATE
3-Indazolecarboxylic acid methyl ester
Indazole-3-carboxylic Acid Methyl Ester
1H-INDAZOLE-3-CARBOXYLIC ACID METHYL ESTER
1H-Indazole-3-Carboxylic Acid Methyl Ester(WX6
methyl 1H-indazole-3-carboxylate(SALTDATA: FREE)
物理化學(xué)性質(zhì)
安全數(shù)據(jù)
制備方法

67-56-1

4498-67-3

43120-28-1
在0℃條件下,將吲唑-3-羧酸(5.0g,30.8mmol)溶解于甲醇(50mL)中,緩慢滴加亞硫酰氯(15mL)。滴加完畢后,將反應(yīng)混合物加熱至回流溫度,并維持該溫度反應(yīng)1.5小時(shí)。反應(yīng)完成后,減壓濃縮反應(yīng)混合物,得到粗產(chǎn)物。向粗產(chǎn)物中加入飽和碳酸氫鈉溶液(50mL)進(jìn)行中和,隨后用乙酸乙酯(50mL×3)進(jìn)行萃取。合并有機(jī)相,用無(wú)水硫酸鈉干燥。過(guò)濾除去干燥劑,減壓濃縮濾液,得到1H-吲唑-3-羧酸甲酯,為白色固體(5.1g,收率94%)。核磁共振氫譜(300MHz,d6-DMSO)數(shù)據(jù)如下:δ 13.91(s,1H),8.06(d,J = 8.2Hz,1H),7.65(d,J = 8.4Hz,1H),7.44(ddd,J = 8.3Hz,6.9Hz,1.1Hz,1H),7.30(dd,J = 7.9Hz,6.9Hz,0.9Hz,1H),3.92(s,3H)。
參考文獻(xiàn):
[1] Tetrahedron Letters, 2007, vol. 48, # 14, p. 2457 - 2460
[2] Chemical Communications, 2010, vol. 46, # 33, p. 6165 - 6167
[3] ChemMedChem, 2017, vol. 12, # 19, p. 1578 - 1584
[4] Patent: WO2013/120104, 2013, A2. Location in patent: Paragraph 00210; 00211
[5] RSC Advances, 2015, vol. 5, # 100, p. 81817 - 81830