Facile, regioselective syntheses of N-alkylated 2,3-diaminopyridines and imidazo[4,5-b]pyridines

DOI: 10.1021/jo00109a029

Source and publish data:

Journal of Organic Chemistry p. 960 - 965 (1995)

Update date:2022-07-31

Topics:

Authors:

Khanna Khanna

Weier Weier

Lentz Lentz

Swenton Swenton

Lankin Lankin

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1021/jo00109a029

Useful strategies are reported for the differentiation and selective synthetic manipulations of amino groups at the 2- and 3-positions of pyridines. It has been found that 2,3-diaminopyridine reacts with aldehydes under reductive amination conditions to g

Full text of DOI:10.1021/jo00109a029

Products guided by the article

Product name:Formamide, N-(3-amino-2-pyridinyl)- (9CI)

Cas No:158525-50-9

R&D Labs maybe for 158525-50-9

Jiangsu Jiuri Chemical Co.,Ltd.

Contact:+86-519-82118868

Address:Tianwang Town, Jurong City, Jiangsu Province, China
China Synchem Technology Co.,Ltd

website:http://www.cnsynchem.com

Contact:+86-0552-4929311

Address:No.217 Daqing Road
Nantong Auxin Electronic Technology Co., LTD

Contact:86-513-88760026

Address:NO.5-1, Aoxin Road, Haian Hi-tech Development Zone, Jiangsu Province, China
Shanghai TBBMed Co.,Ltd

website:http://www.tbbmed.com

Contact:86--21-50498136

Address:Room 6002, Building 7-1, No.160 Basheng Road,Pudong Area,Shanghai China
Lian Xing Chemical Co.,Ltd.

Contact:0792-8228321

Address:10TH Floor No.121 binjiang Road Xunyang District

Relevant to this article

Development of solid-supported Glaser-Hay couplings

Doi:10.1021/co500018k
(2014)
Asymmetric isomerization of ω-hydroxy-α,β-unsaturated thioesters into β-mercaptolactones by a bifunctional aminothiourea catalyst

Doi:10.1021/ol500637x
(2014)
New cinnamic - N-benzylpiperidine and cinnamic - N,N-dibenzyl(N-methyl)amine hybrids as Alzheimer-directed multitarget drugs with antioxidant, cholinergic, neuroprotective and neurogenic properties

Doi:10.1016/j.ejmech.2016.05.055
(2016)
Synthesis of a 2,3-dideoxy-2,3-difluorofuranose with the D-lyxo configuration. An intramolecular rearrangement of methyl 5-O-benzoyl-2,3-dideoxy-2,3-difluoro-D-lyxofuranoside observed during the attempted synthesis of 1-(2,3-dideoxy-2,3-difluoro-β-D-lyxof

Doi:10.1016/0008-6215(94)84007-5
(1994)
Strained Benzene Rings: Preparation and Crystal Structure of a Dithiahexahydro<3.3>paracyclophane, S2C16H22

Doi:10.1021/jo00331a044
(1981)
Synthesis of ethyl ω²H₅-docosa-4,7,10,13,16,19-hexaenoate

Doi:10.1002/jlcr.2580340808
(1994)

Article Doi