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1289386-01-1

(1R,4R)-[4-(3-Nitro-pyridin-2-ylaMino)-cyclohexyl]-carbaMic acid tert-butyl ester synthesis

3synthesis methods
177906-48-8 Synthesis
TRANS-N-BOC-1,4-CYCLOHEXANEDIAMINE

177906-48-8
215 suppliers
$6.00/250mg

(1R,4R)-[4-(3-Nitro-pyridin-2-ylaMino)-cyclohexyl]-carbaMic acid tert-butyl ester

1289386-01-1
7 suppliers
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Yield:1289386-01-1 65%

Reaction Conditions:

with triethylamine in acetonitrile at 85; for 12 h;

Steps:

10.1 (1) Preparation of intermediate XI

1.5 g of 2-fluoro-3-nitropyridine,1.5 g of tert-butyl trans-(4-aminocyclohexyl)carbamate was dissolved in acetonitrile.4 mL of triethylamine was added and reacted at 85 ° C for 12 hours.The reaction solution was cooled to room temperature and concentrated under reduced pressure.Adding an aqueous solution of citric acid, heating and stirring at 30 ° C, and vacuum filtration.The filter cake was washed with a small amount of diethyl ether to give an orange solid, which was intermediate XI.The yield was 65%.

References:

CN109180702,2019,A Location in patent:Paragraph 0152; 0156; 0158; 0166-0169