相似化合物
105250-17-7 13362-28-2 6937-03-7欧盟法规
ECHA物质C&L通报上下游产品
CAS号54221-95-3 2-乙酰基氨基异烟酸 | CAS号6313-54-8 2-氯异烟酸 | CAS号13362-28-2 2-氨基异烟酸 | CAS号64-17-5 乙醇 | CAS号54453-93-9 2-氯异烟酸乙酯 | CAS号695-34-1 2-氨基-4-甲基吡啶 | CAS号5327-32-2 2-(乙酰氨基)-4-甲基吡啶 | CAS号58481-01-9 2-氨基异烟酰肼 | CAS号342613-80-3 咪唑并[1,2-a]吡啶-7-甲醇 | CAS号421595-78-0 Imidazo[1,2-a]p... | CAS号372147-49-4 咪唑并[1,2-a]吡啶-7-甲酸乙酯 | CAS号105250-17-7 2-氨基-4-吡啶甲醇 | CAS号136117-73-2 咪唑并[1,2-a]吡啶-7-甲醛 | CAS号1278407-54-7 2-Phenylimidazo...合成工艺路线路线简述
- 合成目标产物 Ethyl 2-Aminoisonicotinate 主要起始原料 Ethanol And 2-Aminoisonicotinic Acid
- (文献来源)合成步骤主要原料 Ethanol 和 2-Aminoisonicotinic Acid
📜2-(乙酰氨基)-4-甲基吡啶置于盐酸,Potassium Permanganate体系中,化学反应生成2-氨基异烟酸乙酯
参考文献:Synthesis And Sar Of 2-(4-Fluorophenyl)-3-Pyrimidin-4-Ylimidazo[1,2-A]Pyridine Derivatives As Anticoccidial Agents
标题:Synthesis And Sar Of 2-(4-Fluorophenyl)-3-Pyrimidin-4-Ylimidazo[1,2-A]Pyridine Derivatives As Anticoccidial Agents
摘要:Compounds 10A-10D And 10I Are Very Potent Inhibitors Of Eimeria Tenella Cgmp-Dependent Protein Kinase (0.081-0.32 Nm) And Are Very Efficacious Antiparasitic Agents In Vivo When Administered To Chickens At 12.5-25 Ppm Levels In The Feed.
Doi:10.1016/j.Bmcl.2006.08.127
海关参考信息
- 2912110000-甲醛
2915110000-甲酸
2933310010-吡啶
2901100000-饱和无环烃 - 💡 提示:海关信息按照顺序优先匹配,如需确认的海关信息,请参考相关资料。
- 详情请参考:📖 海关编码查询和海关进出口税则
专利信息
专利号:WO-2025128848-A1
优先权日:2023-12-12
标题:Heterocyclic compounds as triggering receptor expressed on myeloid cells 2 agonists and methods of use
发明人:HOUZE JONATHAN B; PANDYA BHAUMIK
权利人:VIGIL NEUROSCIENCE INC
摘要:The present disclosure provides compounds of Formula (I), useful for the activation of Triggering Receptor Expressed on Myeloid Cells 2 ('TREM2'). This disclosure also provides pharmaceutical compositions comprising the compounds, uses of the compounds, and compositions for treatment of, for example, a neurodegenerative disorder. Further, the disclosure provides intermediates useful in the synthesis of compounds of Formula (I).
专利号:US-3901899-A
优先权日:1973-04-27
标题 :Synthesis of indoles from anilines and intermediates therein
发明人:GASSMAN PAUL G
权利人:UNIV OHIO STATE RES FOUND
摘要:Preparing indoles and intermediates therefor by reacting an Nhaloaniline with a Beta -carbonylic hydrocarbon sulfide to form an azasulfonium halide, reacting the azasulfonium halide with a strong base to form a thio-ether indole derivative, and then reducing the thio-ether indole, e.g. with Raney nickel, to form the indole compound. When an acetal or ketal of the Beta carbonyl hydrocarbon sulfide is used, the azasulfonium salt is treated with a base, and then with an acid to form the thio-ether indole derivative. When an Alpha -ethyl- Beta -carbonylic hydrocarbon sulfide is used, the resulting azosulfonium salt reacts with strong base to form a thio-ether indolenine derivative, which on reduction with Raney nickel or complex metal hydrides yields 3-substituted indoles. The aniline may be an aminopyridine to form an aza-indole compound in the process. The azasulfonium salts and thio-ether indole or thio-ether indolenine derivatives can be isolated and recovered from their respective reaction mixtures. The thio-ether-indole and thio-ether indolenine derivatives are useful as intermediates to make the indoles without the thio-ether group. The indoles are known compounds having a wide variety of uses, e.g., in making perfumes, dyes, amino acids, pharmaceuticals, agricultural chemicals and the like.
专利号:US-3992392-A
优先权日:1973-04-27
标题:Synthesis of indoles from anilines and intermediates therein
发明人:GASSMAN PAUL G
权利人:UNIV OHIO STATE RES FOUND
摘要:Preparing indoles and intermediates therefor by reacting an N-haloaniline with a β-carbonylic hydrocarbon sulfide to form an azasulfonium halide, reacting the azasulfonium halide with a strong base to form a thio-ether indole derivative, and then reducing the thio-ether indole, e.g. with Raney nickel, to form the indole compound. When an acetal or ketal of the β-carbonyl hydrocarbon sulfide is used, the azasulfonium salt is treated with a base, and then with an acid to form the thio-ether indole derivative. When an α-ethyl-β -carbonylic hydrocarbon sulfide is used, the resulting azosulfonium salt reacts with strong base to form a thio-ether indolenine derivative, which on reduction with Raney nickel or complex metal hydrides yields 3-substituted indoles. The aniline may be an aminopyridine to form an aza-indole compound in the process. The azasulfonium salts and thio-ether indole or thio-ether indolenine derivatives can be isolated and recovered from their respective reaction mixtures. The thio-ether-indole and thio-ether indolenine derivatives are useful as intermediates to make the indoles without the thio-ether group. The indoles are known compounds having a wide variety of uses, e.g., in making perfumes, dyes, amino acids, pharmaceuticals, agricultural chemicals and the like.
专利号:CA-1043337-A
优先权日:1973-04-27
标题 :Synthesis of indoles from anilines and intermediates therein