ChemicalBook CAS DataBase List (6-BROMO-2-PYRIDINYL)-CARBAMIC ACID,1,1-DIMETHYLETHYL ESTER

(6-BROMO-2-PYRIDINYL)-CARBAMIC ACID,1,1-DIMETHYLETHYL ESTER synthesis

7synthesis methods

Product Name:(6-BROMO-2-PYRIDINYL)-CARBAMIC ACID,1,1-DIMETHYLETHYL ESTER
CAS Number:344331-90-4
Molecular formula:C10H13BrN2O2
Molecular Weight:273.13

19798-81-3

24424-99-5

(6-BROMO-2-PYRIDINYL)-CARBAMIC ACID,1,1-DIMETHYLETHYL ESTER

344331-90-4

Step 1. Synthesis of 6-bromo-2-Boc-aminopyridine: To a solution of dichloromethane (24 mL) containing 6-bromopyridin-2-amine (3 g, 17.34 mmol), triethylamine (3.14 mL, 22.54 mmol), and DMAP (0.424 g, 3.47 mmol) was slowly added a solution of dichloromethane (6 mL) containing di-tert-butyl dicarbonate (4.83 mL, 20.81 mmol). 20.81 mmol) to a solution of dichloromethane (6 mL). The reaction mixture was stirred at room temperature for about 24 hours. Upon completion of the reaction, the reaction mixture was diluted with water, saturated saline and ethyl acetate. The aqueous layer was separated and extracted with ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography to give 6-bromo-2-tert-butoxycarbonylaminopyridine as a white solid. Yield: 1.67 g. LCMS (m/z): 274.9 [M+H]+; Retention time: 0.54 min (major peak), 0.95 min.

19798-81-3 Synthesis

19798-81-3
451 suppliers
$5.00/1g

24424-99-5 Synthesis

24424-99-5
867 suppliers
$13.50/25G

344331-90-4
107 suppliers
$24.00/100mg

Yield: 97%

Reaction Conditions:

with triethylamine in dichloromethane at 20; for 72 h;Product distribution / selectivity;

Steps:

Step 1. Preparation of te/f-butyl 6-bromopyridin-2-ylcarbamateTo a solution of 6-bromopyridin-2-amine (3 g, 17.34 mmol), triethylamine (3.14 mL, 22.54 mmol) and DMAP (0.424 g, 3.47 mmol) in DCM (24 mL) was added slowly a solution of BOC-anhydride (4.83 mL, 20.81 mmol) in DCM (6 mL). The reaction mixture was stirred at ambient temperature for -24 hr. The mixture was diluted with water, brine and EtOAc. The separated aqueous layer was extracted with EtOAc. The combined organic layers were dried over sodium sulfate and concentrated in vacuo. The resulting residue was purified by column chromatography providing te/f-butyl 6-bromopyridin-2- ylcarbamate as a white solid. Yield: 1.67 g. LCMS (m/z): 274.9 [M+H]+; Retention time = 0.95 min.

References:

NOVARTIS AG;ANTONIOS-MCCREA, William R.;BARSANTI, Paul A.;HU, Cheng;JIN, Xianming;LIN, Xiaodong;MARTIN, Eric J.;PAN, Yue;PFISTER, Keith B.;RENHOWE, Paul A.;SENDZIK, Martin;SUTTON, James;WAN, Lifeng WO2012/101066, 2012, A1 Location in patent:Page/Page column 77

21190-87-4 Synthesis