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ETHYL 3-((TERT-BUTOXYCARBONYL)AMINO)CYCLOBUTANECARBOXYLATE synthesis

4synthesis methods
24424-99-5 Synthesis
Di-tert-butyl dicarbonate

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

ETHYL 3-((TERT-BUTOXYCARBONYL)AMINO)CYCLOBUTANECARBOXYLATE

946152-71-2
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Yield:946152-71-2 90%

Reaction Conditions:

in ethanol at 20; for 24 h;

Steps:

24.1

EXAMPLE 24; 3-Acetylamino-cyclobutanecarboxylic acid [3-[5-(4,6-dimethyl-pyrimidine-5-carbonyl)-hexahydro-pyrrolo[3,4-c]pyrrol-2-yl]-1-(3-fluoro-phenyl)-propyl]-amide (I-39) and 3-acetylamino-cyclobutanecarboxylic acid [3-[5-(4,6-dimethyl-pyrimidine-5-carbonyl)-hexahydro-pyrrolo[3,4-c]pyrrol-2-yl]-1-(3-fluoro-phenyl)-propyl]-amide (I-41); Step 1-; 3-Amino-cyclobutanecarboxylic acid ethyl ester (110a, 0.68 g, 4.75 mmol, CAS Reg No. 74307-73-6) and Boc2O (1.24 g, 5.70 mmol) were dissolved in EtOH (120 mL) with stirring. Stirring was continued for 24 h at RT. The reaction mixture was concentrated and residue purified by flash chromatography eluting with 20% EtOAc/hexanes to afford 1.03 g (90%) of 110b as a colorless liquid which solidifies upon standing: MS m/z=266 (M+Na)+.

References:

US2007/191406,2007,A1 Location in patent:Page/Page column 37