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ChemicalBook CAS DataBase List CPI-444

CPI-444 synthesis

3synthesis methods
(S)-7-chloro-3-((6-(((tetrahydrofuran-3-yl)oxy)methyl)pyridin-2-yl)methyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-5-amine

1202402-82-1
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338998-93-9 Synthesis
2-Methylfurane-5-boronic acid pinacol ester

338998-93-9
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Yield:1202402-40-1 90%

Reaction Conditions:

with dichloro[1,1′-bis[bis(1,1-dimethylethyl)phosphino]ferrocene-P,P′]palladium;potassium carbonate in tetrahydrofuran;water at 60;Suzuki Coupling;Temperature;

Steps:

4

The solution of CP-58 (10 g), CP-60 (6.9 g) , Pd(dtbpf)C12 (approx. 0.0015 mol eq) and K2C03 (5.8 g) in THF (6V) and H20 (3V) is heated to approximately 60 °C. The reaction is complete after approximately 30 minutes. The solution is cooled to 50 °C and aqueous layer is separated. The aqueous layer is extracted with THF (9 mL); the THF layer is added to organic solution. The organics are cooled to 40 °C, 1 ,3-diaminopropane (DAP; approximately 50 g) or ethylene diamine (EDA; approximately 45 g) is added and the mixture stined for 1 hour. H20 (15V) is added to the organic layer over 10 mm. The sluny is cooled to 20 °C for 2 hours, and stined for an additional 1 hour. The sluny is filtered and washed with H20 (2V x 2) and iPrOH (lv). CPI-444 wet-cake is dried at 50 °C under full vacuum. (Yield = 90 %; purity> 99.0%)

References:

WO2018/183965,2018,A1 Location in patent:Paragraph 0350; 0351; 0352; 0353; 0354

1202402-79-6 Synthesis
(S)-(6-((tetrahydrofuran-3-yloxy)methyl)pyridin-2-yl)methanamine

1202402-79-6
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