(3-IODO-PYRIDIN-4-YL)-CARBAMIC ACID TERT-BUTYL ESTER Chemical Properties

Melting point:

79-83°C

Boiling point:

313.2±27.0 °C(Predicted)

Density 

1.652±0.06 g/cm3(Predicted)

storage temp. 

under inert gas (nitrogen or Argon) at 2–8 °C

form 

solid

pka

11.85±0.70(Predicted)

color 

White

Sensitive 

Light Sensitive

CAS DataBase Reference

211029-67-3(CAS DataBase Reference)

Safety Information

HS Code 

2924190091

(3-IODO-PYRIDIN-4-YL)-CARBAMIC ACID TERT-BUTYL ESTER Usage And Synthesis

Synthesis

General procedure for the synthesis of 4-(Boc-amino)-3-iodopyridine from 4-(tert-butoxycarbonylamino)pyridine: n-butyllithium (1.6 M hexane solution, 220 ml, 0.35 mol) was added slowly and dropwise over a period of 30 min to a stirred solution of 4-(tert-butoxycarbonylamino)pyridine (26.08 g, 0.13 mol) and N,N,N' ,N'-tetramethylethylenediamine (55 ml, 0.36 mol) in a solution of tetrahydrofuran (750 ml). The reaction mixture was stirred at -78°C for 15 minutes, followed by warming to -10°C and continued stirring for 2 hours. The reaction mixture was re-cooled to -78°C and a solution of iodine (95.11 g, 0.37 mol) in tetrahydrofuran (250 ml) was added dropwise over 30 minutes. After the dropwise addition, the mixture was continued to be stirred at -78°C for 2 hours. Upon completion of the reaction, the reaction mixture was cooled to 0°C using an ice water bath and the reaction was quenched by the slow addition of water (250 ml). Saturated sodium sulfite solution (100 ml) was then added and the organic layer was separated. The aqueous layer was extracted with dichloromethane (2 x 500 ml), the organic layers were combined, dried with anhydrous sodium sulfate and concentrated under reduced pressure to give a brown oil. The crude product was purified by silica gel fast column chromatography with 20% ethyl acetate/heptane as eluent to afford tert-butyl (3-iodopyridin-4-yl)-carbamate (25.00 g, 58%) as an off-white solid.1H NMR (400 MHz, CDCl3) δ 8.76 (1H, s), 8.35 (1H, d, J = 5.7 Hz), 8.11 (1H , d, J = 5.7 Hz), 7.04 (1H, br s), 1.55 (9H, s); retention time (Tr) = 0.99 min, m/z (ES+) (M+H)+ 321.08.

References

[1] Patent: WO2005/121141, 2005, A1. Location in patent: Page/Page column 13; 20
[2] Journal of Organic Chemistry, 2004, vol. 69, # 20, p. 6772 - 6780

(3-IODO-PYRIDIN-4-YL)-CARBAMIC ACID TERT-BUTYL ESTER(211029-67-3)Related Product Information

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