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188057-42-3

2-Azabicyclo[2.2.1]heptane-2,3-dicarboxylic acid, 2-(1,1-diMethylethyl) 3-ethyl ester, (1R,3S,4S)- synthesis

6synthesis methods
24424-99-5 Synthesis
Di-tert-butyl dicarbonate

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214910-41-5 Synthesis
2-Azabicyclo[2.2.1]heptane-3-carboxylicacid,ethylester,(1R,3S,4S)-(9CI)

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2-Azabicyclo[2.2.1]heptane-2,3-dicarboxylic acid, 2-(1,1-diMethylethyl) 3-ethyl ester, (1R,3S,4S)-

188057-42-3
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Yield:188057-42-3 95%

Reaction Conditions:

with triethylamine in tetrahydrofuran;water at 20; for 40 h;

Steps:

5

Step5: To R5G in a solution of triethylamin (24.6 ml), THF (150 ml) and water (2ml), R5I (15.9 g; 73 mmol) is added and the resulting mixture stirred for 40hours at room temperature, then concentrated in vacuo. Ethyl acetate is added to the residue, subsequently extracted with water, 1 N acidic acid and water, before the organic layer is dired over MgS04 and concentrated in vacuo to yield R5I. (Yield 95% m/z 270 [M+H]+, rt 1.33 min, LC-MS Method V003_003).

References:

WO2014/140075,2014,A1 Location in patent:Page/Page column 198-200

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2-Azabicyclo[2.2.1]heptane-2,3-dicarboxylic acid, 2-(1,1-diMethylethyl) 3-ethyl ester, (1R,3S,4S)-

188057-42-3
5 suppliers
inquiry