反应详情

A solution of 2-chloro-5-nitropyridine (3.16 g, 20 mmol) in dry acetonitrile (40 ml) was added dropwise to a solution of 1,3-diaminopropane (5.0 ml) in acetonitrile (20 ml) at room temperature. After 7.5 hour, a yellow solid precipitated in the reaction mixture. The solvent was removed in vacuo and the residue was partitioned between 2.5 M aqueous sodium hydroxide and dichloromethane. The layers were separated and the aqueous portion was extracted 3× with dichloromethane. The combined organic layers were back-extracted with a saturated sodium chloride solution, then dried and concentrated in vacuo using a Buchi rotary evaporator Model R-124 to give (3-aminopropyl)(5-nitro (2-pyridyl))amine as a yellow solid (2.55 g). The amine (1.14 g, 6 mmol) was shaken with benzotriazole carboxamidinium 4-methylbenzenesulfonate (2.0 g, 6 mmol) and diisopropylethyl amine (DIEA) (1.05 ml, 6 mmol) in acetonitrile (10 ml) at room temperature over two days. Dilution with ether gave the amino-{3-[(5-nitro (2-pyridyl))amino]propyl}carboxamidinium 4-methylbenzenesulfonate as a solid.

1. customa yellow solid precipitated in the reaction mixture
2. customThe solvent was removed in vacuo
3. customthe residue was partitioned between 2.5 M aqueous sodium hydroxide and dichloromethane
4. customThe layers were separated
5. extractionthe aqueous portion was extracted 3× with dichloromethane
6. extractionThe combined organic layers were back-extracted with a saturated sodium chloride solution
7. customdried
8. concentrationconcentrated in vacuo
9. customa Buchi rotary evaporator Model R-124