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・ 2-amino-5-formylamino-6-ribosylaminopyrimidin-4(3H)-one 5'-monophosphate deformylase
・ 2-Aminoacridine
・ 2-aminoadipate transaminase
・ 2-aminobenzenesulfonate 2,3-dioxygenase
・ 2-Aminoethoxydiphenyl borate
・ 2-aminoethylphosphonate—pyruvate transaminase
・ 2-aminohexano-6-lactam racemase
・ 2-aminohexanoate transaminase
・ 2-Aminoindane
・ 2-Aminoisobutyric acid
・ 2-aminomuconate deaminase
・ 2-Aminomuconic acid
・ 2-Aminomuconic semialdehyde
・ 2-Aminophenol
・ 2-Aminopurine
2-Aminopyridine
・ 2-Aminotetralin
・ 2-Arachidonoylglycerol
・ 2-Arachidonyl glyceryl ether
・ 2-Azetidinone
・ 2-Benzylpiperidine
・ 2-bit
・ 2-bridge knot
・ 2-Bromo-1-chloropropane
・ 2-Bromo-4,5-methylenedioxyamphetamine
・ 2-Bromo-LSD
・ 2-Bromobutane
・ 2-Bromobutyric acid
・ 2-Bromohexane
・ 2-Bromomescaline


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2-Aminopyridine : ウィキペディア英語版
2-Aminopyridine

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2-Aminopyridine is an organic compound with the formula H2NC5H4N. It is one of three isomeric aminopyridines. It is a colourless solid that is used in the production of the drugs piroxicam, sulfapyridine, tenoxicam, and tripelennamine. It is produced by the reaction of sodium amide with pyridine, the Chichibabin reaction.〔Shinkichi Shimizu, Nanao Watanabe, Toshiaki Kataoka, Takayuki Shoji, Nobuyuki Abe, Sinji Morishita, Hisao Ichimura "Pyridine and Pyridine Derivatives" in Ullmann's Encyclopedia of Industrial Chemistry 2000, Wiley-VCH, Weinheim. 〕
==Structure==
Although 2-hydroxypyridine exists in significant amounts as the pyridone tautomer, the related imine tautomer (HNC5H4NH) is less important for 2-aminopyridine.

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