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3-吡啶硼酸頻那醇酯的合成及其應(yīng)用

2022/9/5 13:42:13

基本描述

3-吡啶硼酸頻那醇酯呈白色結(jié)晶粉末,它的CAS號(hào)是329214-79-1,分子式為C11H16BNO2,以及分子量是205.06。熔點(diǎn)102-104.4°C(lit.)沸點(diǎn)是300.9±15.0°C(Predicted),密度為1.03±0.1g/cm3(Predicted)以及酸度系數(shù)(pKa)是5.22±0.12(Predicted)。3-吡啶硼酸頻那醇酯作為醫(yī)藥中間體占有重要的地位,在臨床上具有潛在的生物活性[1]。

1.png

圖1 3-吡啶硼酸頻那醇酯的結(jié)構(gòu)式。

合成

2.png

圖2 3-吡啶硼酸頻那醇酯的合成路線[2]。

在25ml圓底燒瓶中稱(chēng)量B2pin2(279mg,1.1mmol)和2-氨基苯甲腈(1aa,118mg,1.0mmol)。然后依次加入MeCN(3毫升)和叔丁腈(2a,155毫克,1.5毫摩爾)。將所得反應(yīng)溶液在80°C下攪拌2小時(shí)(在5至15分鐘內(nèi)完成N2析出)。然后在減壓下濃縮溶液,并通過(guò)快速色譜法(硅膠,石油醚/EtOAc=200:1)純化粗殘留物。得到2-(4,4,5,5-四甲基-1,3,2-二氧苯并呋喃-2-基)苯甲腈(4aa)11(152mg,66%),為淡黃色固體。表1.2-氨基苯甲腈條目6 3-(4,4,5,5-四甲基-1,3,2-二氧苯并呋喃-2-基)吡啶(5dd)19的反應(yīng)條件優(yōu)化,從環(huán)己烷重結(jié)晶得到5dd。白色固體3-吡啶硼酸頻那醇酯(123毫克,60%) mp 99 101 °C. 1H NMR (400 MHz, CDCl3) δ 8.95 (s, 1H), 8.69 8.65 (m, 1H), 8.06 (d, J = 7.5 Hz, 1H), 7.30 7.27 (m, 1H), 1.36 (s, 12H); 13C NMR (100 MHz, CDCl3) δ 155.3, 151.8, 142.2, 123.0, 84.2, 24.8; IR (film) 2976 (w), 1474 (m), 1413 (m), 1363 (m), 1156 (s), 1048 (s), 1024 (m), 876 (m), 734 (m) cm 1; EITheMS (m/z, 相對(duì)強(qiáng)度) 205 (M+, 36), 190 (100), 148 (44), 120 (15), 106 (87), 105 (33).

 3.png

圖3 3-吡啶硼酸頻那醇酯的合成路線[3]。

將干燥的二乙醚(約200ml)和正丁基鋰(25.0ml,66.5mmol)的己烷溶液(2.66M)加入到充滿氮?dú)鈿夥盏?頸300ml玻璃燒瓶中。在-80°C下,將3-溴吡啶(9.562 g,60.52 mmol)的乙醚溶液(約30 mL)緩慢添加到溶液中。在-80°C下攪拌混合物30分鐘后,在相同溫度下將三甲氧基硼烷(8.00 mL,73.4 mmol)緩慢添加到混合物中。當(dāng)反應(yīng)溶液升溫至室溫1d時(shí),向溶液中加入吡那醇(7.549g,63.89mmol),然后在室溫下攪拌該溶液1h。向溶液中加入乙酸(7.70毫升,0.135摩爾),然后在室溫下將溶液攪拌6小時(shí)。在減壓下濃縮混合物。粗產(chǎn)物用CH2Cl2萃取,然后用冷CH3CN和己烷洗滌所得固體,得到白色固體的3-吡啶硼酸吡那醇酯(10.640g,51.869mmol,86%)3-吡啶硼酸頻那醇酯,產(chǎn)率10.640g,51.869mmol,86%。1H NMR(400MHz,CDCl3,rt):δ1.35(s,12H),7.27(dd,J=4.6,8.2 Hz,1H),8.05(dd,J=1.6,1.2 Hz),8.66(dd,i=1.4,4.6 Hz,1H),8.94(s,1H)。

4.png

 圖4 3-吡啶硼酸頻那醇酯的合成路線[4]。

入無(wú)水四氫呋喃(THF, 5 ml),加入2-異丙基-4,4,5,5-四甲基-1,3,2-二氧硼烷(1.5 mmol)。最后,在得到的混合物中加入1,2-二溴乙烷(1.0 mmol)。反應(yīng)混合物在室溫下攪拌3小時(shí)。反應(yīng)完成后,將反應(yīng)混合物抽吸過(guò)濾,收集濾液。濾液加入飽和NaCl溶液(20 ml)后,用二氯甲烷(CH2Cl2, 20 ml)多次萃取。將有機(jī)層分離,在硫酸鎂上干燥,減壓濃縮,除去溶劑,得到純化產(chǎn)物。例2的步驟重復(fù),只是將1,2-二聚甲烷替換為1,2-二碘乙烷、碘、劉易斯酸等其他活化劑;金屬選擇Mg、Li、Zn、Cu或Cu/Zn合金;醚代替四氫呋喃作為溶劑。得到最終產(chǎn)品3-吡啶硼酸頻那醇酯。光譜數(shù)據(jù)如下:1H-NMR (300 MHz, CDCl3): δ 1.34 (12H, s), δ 7.24 (1H, m), δ 7.81 (1H, m), δ 8.62 (1H, dd, J = 1.78, 4.8), δ 8.69 (1H, s); 13C-NMR (75.5 MHz, CDCl3): δ 25.1, δ 84.2, δ 123.2, δ 142.4, δ 151.5, δ 155.1; IR(Neat): 3005 (m), 2989 (m), 1275 (s), 1260 (s), 1143 (m); C11H16BNO2; MW: 205.0612.

應(yīng)用

3-吡啶硼酸頻那醇酯具有特殊的化學(xué)性質(zhì)和藥用活性,是許多醫(yī)藥、農(nóng)藥的中間體,應(yīng)用前景非常廣闊[5-7]。其還可用作醫(yī)藥及醫(yī)藥中間體、染發(fā)助劑、聚和物穩(wěn)定劑、感光材料的抗氧化劑和抗灰霧劑等等[8]。

儲(chǔ)存條件

3-吡啶硼酸頻那醇酯必須密封避光保存,不可與空氣接觸。同時(shí)必須儲(chǔ)存于陰涼、通風(fēng)的庫(kù)房,遠(yuǎn)離火種和熱源以及強(qiáng)堿性試劑。庫(kù)房溫度不可溫度過(guò)高,一般超過(guò)26℃。3-吡啶硼酸頻那醇酯應(yīng)與氧化劑等分開(kāi)存放,切忌混儲(chǔ),不宜大量?jī)?chǔ)存或久存[9-10]。

風(fēng)險(xiǎn)描述

3-吡啶硼酸頻那醇酯能夠腐蝕皮膚表面,一旦被皮膚接觸到立刻脫去被污染的衣物,用肥皂水和清水徹底沖洗皮膚。如果3-吡啶硼酸片吶被眼睛接觸到,應(yīng)該提起眼瞼,用流動(dòng)的清水或者氯化鈉生理鹽水沖洗,然后迅速就醫(yī)。一旦不小心被吸入3-吡啶硼酸頻那醇酯的揮發(fā)性氣體,應(yīng)該迅速逃脫現(xiàn)場(chǎng)移動(dòng)到空氣新鮮處。保持呼吸道暢通。

參考文獻(xiàn)

[1] U. Balijapalli, R. Nagata, Y. Tsuchiya, H. Nakanotani, C. Adachi, Dibenzopyrazine derivative, light-emitting material, delayed fluorescence material, and organic light-emitting element, Kyulux Co., Ltd., Japan . 2022, p. 64pp.; Chemical Indexing Equivalent to 178:378075 (WO).

[2] U. Balijapalli, R. Nagata, Y. Tsuchiya, H. Nakanotani, C. Adachi, Dibenzopyrazine derivative, light-emitting material, delayed fluorescence material, and organic light-emitting element, Kyulux, Inc., Japan . 2022, p. 100pp.; Chemical Indexing Equivalent to 179:9385 (JP).

[3] C. Chen, C. Wang, H. Lin, X. Du, Y. Che, Preparation of 2-methoxy-3-amino-5-pyridine boronic acid pinacol ester and its intermediates, Hangzhou Zhulian Pharmaceutical Technology Co., Ltd., Peop. Rep. China . 2022, p. 9pp.

[4] C. Huang, Y. Wu, N. Zhai, X. Ju, C. Zhao, X. Luo, Y. Ozoe, G. Liu, 5-(4-Pyridinyl)-3-isothiazolols as Competitive Antagonists of Insect GABA Receptors: Design, Synthesis, and a New Mechanism Leading to Insecticidal Effects, J. Agric. Food Chem. 70(19) (2022) 5765-5772.

[5] L. Ji, B. Park, H. Zhao, Boron-containing chemicals as cathode additives, Si anode additives, electrolyte additives or separator modifiers for Li-ion batteries, Enevate Corporation, USA . 2022, p. 82pp.; Chemical Indexing Equivalent to 178:263497 (US).

[6] Y. Ouyang, H. Si, C. Zhu, L. Zhong, H. Ma, Z. Li, H. Xiong, T. Liu, Z. Liu, Z. Zhang, Z.-M. Zhang, Q. Cai, Discovery of 8-(6-Methoxypyridin-3-yl)-1-(4-(piperazin-1-yl)-3-(trifluoromethyl)phenyl)-1,5-dihydro-4H-[1,2,3]triazolo[4,5-c]quinolin-4-one (CQ211) as a Highly Potent and Selective RIOK2 Inhibitor, J. Med. Chem. 65(11) (2022) 7833-7842.

[7] Y. Qu, N. Jiang, W. Huang, Y. Wang, A. Lv, Y. Jin, Y. Liu, Y. Lan, K. Dong, Preparation method of dipyridine triphenylamine aldehyde fluorescent material with aggregation-induced luminescence effect, and its application in fingerprint enhancement and latent fingerprint imaging, Shanghai University of Engineering Science, Peop. Rep. China . 2022, p. 17pp.

[8] N. Sokolova, K. McCormack, G. Henkel, V.R. Gantla, E. Brown, Preparation of imidazopyridines as sodium channel modulators, Arisan Therapeutics Inc., USA . 2022, p. 200pp.

[9] L. Sun, Z. Pang, M. Duan, W. Zhang, J. Lv, Q. Tong, S. Wei, Y. Liu, X. Chen, C. Sun, Preparation method of torezolid [Machine Translation], Hebei Guangxiang Pharmaceutical Co., Ltd., Peop. Rep. China . 2022, p. 8pp.

[10] T.J. Troxler, D. Orain, P. Furet, K. Weigand, A. Schlapbach, Pyridine derivatives as interleukin-17 inhibitors and their preparation, Novartis AG, Switz. . 2022, p. 232pp.

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