934-37-2 (2-甲基咪唑并[1,2-a]吡啶,2-Methylimidazo[1,2-A]pyridine)

CAS号:
934-37-2
中文名称:
2-甲基咪唑并[1,2-a]吡啶
英文名称:
2-Methylimidazo[1,2-A]pyridine
分子式:
C8H8N2
分子量:
132.162521362305

2-甲基咪唑并[1,2-a]吡啶(934-37-2)名称与标识符

名称

中文别名:
2-甲基咪唑并[1,2-a]吡啶;
英文别名:
2-Methylimidazo[1,2-a]pyridine;Imidazo[1,2-a]pyridine, 2-methyl-;2-methylH-imidazo[1,2-a]pyridine;2-Methylimidazo(1,2-a)pyridine;2-Methyl-imidazo[1,2-a]pyridin;2-Methyl-Imidazo[1,2-a]pyridine;IMIDAZO[1,2-A]PYRIDINE,2-METHYL-;methylimidazo[1,2-a]pyridine;BZACBBRLMWHCNM-UHFFFAOYSA-N;2-methylimidazo (1,2-a)pyridine;2-methylimidazo(1,2-a) pyridine;SBB056298;MB02386;CM10614;2-methyl-4-hydroimidazo[1,2-a]pyridine;AB0039131;2-Methylimidazo[1,2-a]pyridine (ACI);Imidazo[1,2-a]pyridine, 2-methyl-;2-Methylimidazo[1,2-a]pyridine;;SCHEMBL171008;EN300-18552;Z82176792;CS-0006838;DTXCID80161901;TS-01714;SY107161;DTXSID60239410;934-37-2;AKOS003614801;MFCD02251330;

标识符

MDL:
MFCD02251330
InChIKey:
BZACBBRLMWHCNM-UHFFFAOYSA-N
Inchi:
1S/C8H8N2/c1-7-6-10-5-3-2-4-8(10)9-7/h2-6H,1H3
SMILES:
N1C(C)=CN2C=1C=CC=C2

2-甲基咪唑并[1,2-a]吡啶(934-37-2)物化性质

实验特性

  • LogP : 1.64270
  • PSA : 17.30000
  • 水溶性 : Slightly soluble in water.
  • 沸点 : 148℃/20mm
  • 熔点 : 391-394 ºC
  • 溶解度 : 微溶 (2.4 g/L) (25 ºC),
  • 敏感性 : Hygroscopic
  • 密度 : 1.11±0.1 g/cm3 (20 ºC 760 Torr),

计算特性

  • 精确分子量 : 132.06900
  • 氢键供体数量 : 0
  • 氢键受体数量 : 1
  • 可旋转化学键数量 : 0
  • 同位素质量 : 132.068748264g/mol
  • 重原子数量 : 10
  • 复杂度 : 124
  • 同位素原子数量 : 0
  • 确定原子立构中心数量 : 0
  • 不确定原子立构中心数量 : 0
  • 确定化学键立构中心数量 : 0
  • 不确定化学键立构中心数量 : 0
  • 共价键单元数量 : 1
  • 疏水参数计算参考值(XlogP) : 2.2
  • 拓扑分子极性表面积 : 17.3

2-甲基咪唑并[1,2-a]吡啶(934-37-2)海关数据

海关编码:
2933990090
海关数据:

中国海关编码:

2933990090

概述:

2933990090. 其他仅含氮杂原子的杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

申报要素:

品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期

Summary:

2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

2-甲基咪唑并[1,2-a]吡啶(934-37-2)推荐厂家 更多厂家(15)

2-甲基咪唑并[1,2-a]吡啶(934-37-2)合成路线

合成路线:1 步
反应条件:
参考文献:
Rapid, metal-free and aqueous synthesis of imidazo[1,2-a]pyridine under ambient conditions
Chapman, Michael R.; Kwan, Maria H. T.; King, Georgina E.; Kyffin, Benjamin A.; Blacker, A. John; et al, Green Chemistry, 2016, 18(17), 4623-4627
合成路线:1 步
反应条件:
参考文献:
Process for the manufacture of 6-alkynyl-pyridine derivatives
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Synthesis of 2-Carbonylimidazo[1,2-a]pyridines via Iodine-mediated Intramolecular Cyclization of 2-Amino-N-propargylpyridinium Bromides
Pandey, Khima; Kaswan, Pinku; Saroj; Kumar, Anil, ChemistrySelect, 2016, 1(21), 6669-6672
合成路线:1 步
反应条件:
参考文献:
Synthesis and halogenation of 2-methylimidazo[1,2-a]pyridine. Antimicrobial activity of 3-bromo-2-methyl-1H-imidazo[1,2-a]pyridinium bromide
Kalita, Elena V.; Kim, Dmitry G.; Krynina, Elizaveta M.; Sharutin, Vladimir V.; Shlepotina, Nina M.; et al, Chemistry of Heterocyclic Compounds (New York, 2022, 58(4-5), 227-234
合成路线:1 步
反应条件:
参考文献:
Preparation of indole and imidazo[1,2-a]pyridine compounds as neuropeptide S antagonists for the treatment of addictive disorders, mood, anxiety and sleep disorders
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Structure-Activity Relationship of Imidazopyridinium Analogues as Antagonists of Neuropeptide S Receptor
Patnaik, Samarjit; Marugan, Juan J.; Liu, Ke; Zheng, Wei; Southall, Noel; et al, Journal of Medicinal Chemistry, 2013, 56(22), 9045-9056
合成路线:1 步
反应条件:
参考文献:
Metal free coupling of heteroaryl N-tosylhydrazones and thiols: Efficient synthesis of sulfides
Garcia-Carrillo, Mario Alfredo; Guzman, Angel; Diaz, Eduardo, Tetrahedron Letters, 2017, 58(20), 1952-1956
合成路线:1 步
反应条件:
参考文献:
Electrochemically initiated intermolecular C-N formation/cyclization of ketones with 2-aminopyridines: an efficient method for the synthesis of imidazo[1,2-a]pyridines
Feng, Mei-Lin; Li, Shu-Qi; He, Hui-Zi; Xi, Long-Yi; Chen, Shan-Yong; et al, Green Chemistry, 2019, 21(7), 1619-1624
合成路线:1 步
反应条件:
参考文献:
Pd-Cu catalyzed heterocyclization during Sonogashira coupling: synthesis of 2-benzylimidazo[1,2-a]pyridine
Bakherad, Mohammad; Nasr-Isfahani, Hossein; Keivanloo, Ali; Doostmohammadi, Nesa, Tetrahedron Letters, 2008, 49(23), 3819-3822
合成路线:1 步
反应条件:
参考文献:
Imidazopyridinyl thiazolyl compounds as histone deacetylase inhibitors and their preparation and use in the treatment of diseases
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Aerobic Multicomponent Tandem Synthesis of 3-Sulfenylimidazo[1,2-a]pyridines from Ketones, 2-Aminopyridines, and Disulfides
Ge, Wenlei; Zhu, Xun; Wei, Yunyang, European Journal of Organic Chemistry, 2013, 2013(27), 6015-6020
合成路线:1 步
参考文献:
Metal-Free Mediated C-3 Methylsulfanylation of Imidazo[1,2-a]-pyridines with Dimethyl Sulfoxide as a Methylsulfanylating Agent
Chen, Zhengkai ; Cao, Gangjian; Zhang, Fengjin; Li, Hongli; Xu, Jianfeng ; et al, Synlett, 2017, 28(14), 1795-1800
合成路线:1 步
反应条件:
参考文献:
The imidazopyridine derivative JK184 reveals dual roles for microtubules in hedgehog signaling
Cupido, Tommaso; Rack, Paul G.; Firestone, Ari J.; Hyman, Joel M.; Han, Kyuho; et al, Angewandte Chemie, 2009, 48(13), 2321-2324
合成路线:1 步
反应条件:
参考文献:
Copper(I) Iodide-Catalyzed Aerobic Oxidative Synthesis of Imidazo[1,2-a]pyridines from 2-Aminopyridines and Methyl Ketones
Chandra Mohan, Darapaneni; Reddy Donthiri, Ramachandra; Nageswara Rao, Sadu; Adimurthy, Subbarayappa, Advanced Synthesis & Catalysis, 2013, 355(11-12), 2217-2221
合成路线:1 步
反应条件:
参考文献:
Synthesis and cytotoxic activity of 2-methylimidazo[1,2-a]pyridine- and quinoline-substituted 2-aminopyrimidine derivatives
Vilchis-Reyes, Miguel Angel; Zentella, Alejandro; Martinez-Urbina, Miguel Angel; Guzman, Angel; Vargas, Omar; et al, European Journal of Medicinal Chemistry, 2010, 45(1), 379-386
合成路线:1 步
反应条件:
参考文献:
Preparation of fused heterocyclic imidazolyl compounds for treatment of HDAC- and CDK-mediated diseases
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Discovery of a First-in-Class, Potent, Selective, and Orally Bioavailable Inhibitor of the p97 AAA ATPase (CB-5083)
Zhou, Han-Jie; Wang, Jinhai; Yao, Bing; Wong, Steve; Djakovic, Stevan; et al, Journal of Medicinal Chemistry, 2015, 58(24), 9480-9497
合成路线:1 步
反应条件:
参考文献:
Electrochemically Promoted [3+2] Annulation of Imidazo[1,2-a]pyridine with Alkynes
Ping, Meng-Qi; Guo, Ming-Zhong; Li, Rui-Tao; Wang, Zi-Chen; Ma, Cheng; et al, Organic Letters, 2022, 24(40), 7410-7415
合成路线:1 步
反应条件:
参考文献:
Unconventional Reactivity with DABCO-Bis(sulfur dioxide): C-H Bond Sulfenylation of Imidazopyridines
Le Bescont, Julie; Breton-Patient, Chloe; Piguel, Sandrine, European Journal of Organic Chemistry, 2020, 2020(14), 2101-2109
合成路线:1 步
反应条件:
参考文献:
Identification of the Privileged Position in the Imidazo[1,2-a]pyridine Ring of Phosphonocarboxylates for Development of Rab Geranylgeranyl Transferase (RGGT) Inhibitors
Kazmierczak, Aleksandra; Kusy, Damian; Niinivehmas, Sanna P.; Gmach, Joanna; Joachimiak, Lukasz ; et al, Journal of Medicinal Chemistry, 2017, 60(21), 8781-8800

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