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HRID2421692

反应详情

EQUATION

反应方程式

HRID 2421692 的结构方程式

REACTANTS

反应物

2
结构：CC(C)(C)OC(=O)NC1CCNCC1
HCID723833

4-(N-Boc-amino)piperidine

C10H20N2O2

结构：O=C(O)c1ccncc1Nc1ccc(I)cc1F
HCID59026791

3-(2-Fluoro-4-iodoanilino)pyridine-4-carboxylic acid

C12H8FIN2O2

2 次

PRODUCTS

生成物

1
结构：CC(C)(C)OC(=O)NC1CCN(C(=O)c2ccncc2Nc2ccc(I)cc2F)CC1
HCID11497541

未命名化合物

PROCEDURE

实验过程

tert-butyl(1-{3-[(2-fluoro-4-iodophenyl)amino]isonicotinoyl}piperidin-4-yl)carbamate was synthesized according to the procedure for General Method 1, outlined above, starting with 2.4 mmol of 3-[(2-fluoro-4-iodophenyl)amino]isonicotinic acid (intermediate 1) and 4.0 mmol of piperidin-4-yl-carbamic acid tert-butyl ester. LC/MS [9.47 min; 541 (M+1)]

WORKUP

后处理

  1. customLC/MS [9.47 min; 541 (M+1)]