2-Chloroisonicotinic acid → tert-Butyl 2-chloropyridine-4-carboxylate

A 1-L jacketed 3-neck round bottom flask equipped with overhead stirrer, N2-inlet vented to the atmosphere and thermocouple was charged with 2-chloroisonicotinic acid (78.0 g, 495 mmol), di-tert-t-butyl dicarbonate (230.1 g, 1054 mmol), and 1-methyl-2-pyrrolidinone (179.3 g). A solution of 4-dimethylamino pyridine (11.61 g, 95 mmol) dissolved in 1-methyl-2-pyrrolidinone (60.0 g) was charged to the mixture and the temperature was adjusted to 25±10° C. The reaction was quenched after stirring for about 17 hours by the addition of an ice-cold solution of sodium chloride (30.0 g) and monobasic potassium phosphate (30.2 g) in water (320.7 g). Methyl tert-butyl ether (278 g) was added, and the mixture was stirred and allowed to settle. The layers were separated. The organic phase was washed three times with water (˜230-240 g each) then diluted with toluene (239 g) and distilled under vacuum to a red oil (150.8 g, KF 29.9 ppm H2O). 1H NMR (400 MHz, CDCl3) δ ppm 1.60 (s, 9H) 7.69-7.72 (m, 1H) 7.79-7.81 (m, 1H) 8.49 (dd, J=5.08, 0.69 Hz, 1H).

1. customA 1-L jacketed 3-neck round bottom flask equipped with overhead stirrer, N2-inlet
2. additionwas charged to the mixture
3. customwas adjusted to 25±10° C
4. customThe reaction was quenched
5. additionMethyl tert-butyl ether (278 g) was added
6. stirringthe mixture was stirred
7. customThe layers were separated
8. washThe organic phase was washed three times with water (˜230-240 g each)
9. additionthen diluted with toluene (239 g)
10. distillationdistilled under vacuum to a red oil (150.8 g, KF 29.9 ppm H2O)

ORD record

ord-7f9b5a06ffb9489cad0d4aa3306c7b86

Source dataset

uspto-grants-2016_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09260411B2