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ChemicalBook CAS DataBase List Cetilistat

Cetilistat synthesis

6synthesis methods
Commercially available hexadecanol (21) was treated with phosgene in THF/toluene to give the corresponding chloroformate (22), which was immediately subjected to commercial 2-amino-5- methylbenzoic acid (23) in pyridine. Subsequent slow addition of methyl chloroformate at room temperature resulted in the formation of cetilistat (IV), which was produced in 31% overall yield from hexadecanol.

890655-08-0 Synthesis
Cetilistat Intermediate

890655-08-0
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Yield:282526-98-1 96.5%

Reaction Conditions:

with 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride in dichloromethane at 20;Solvent;Reagent/catalyst;

Steps:

5 Example 5 Synthesis of Cetilistat

In a 3L three-mouth flask, disperse the compound C (120g) in 2L dichloromethane. Under stirring add EDCI (82.24g). The reaction was stirred at room temperature.TLC (n-hexane: ethyl acetate: acetic acid = 50:1:0.1) monitored the progress of the reaction, the reaction was complete after washing 3 times × 700mL, the organic layer was separated, 12g of activated carbon was added and refluxed for 20min, cooled to room temperature activated carbon was filtered off , concentrated under reduced pressure to remove methylene chloride, the crude product was dispersed in 575mL of acetonitrile, stirred at room temperature for 1 hour to fully disperse the substrate, an ice-water bath (0-10 deg.C) was stirred for 3 hours, filtration, 40 deg.C blast drying, a white solid 110.8g. Yield 96.5%.

References:

CN105669585,2016,A Location in patent:Paragraph 0063; 0064; 0065

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