Reaktion #60015

Reaktionsgleichung

2-chloro-5-nitropyridine

1,3-diaminopropane

→

(3-aminopropyl)(5-nitro(2-pyridyl))amine

Lösungsmittel

acetonitrile

acetonitrile

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigea yellow solid precipitated in the reaction mixture
2. 2
   SonstigeThe solvent was removed in vacuo
3. 3
   Sonstigethe residue was partitioned between 2.5 M aqueous sodium hydroxide and dichloromethane
4. 4
   SonstigeThe layers were separated
5. 5
   Extraktionthe aqueous portion was extracted 3× with dichloromethane
6. 6
   ExtraktionThe combined organic layers were back-extracted with a saturated sodium chloride solution
7. 7
   Sonstigedried
8. 8
   Einengenconcentrated in vacuo
9. 9
   Sonstigea Buchi rotary evaporator Model R-124

Vorschrift

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.

Quelle