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ChemicalBook CAS DataBase List REMODULIN

REMODULIN synthesis

8synthesis methods
-

Yield:81846-19-7 91%

Reaction Conditions:

with hydrogenchloride in water;ethyl acetate; pH=1 for 0.166667 h;Product distribution / selectivity;

Steps:

5
A 250-mL, round-bottom flask equipped with magnetic stirrer was charged with treprostinil diethanolamine salt (4 g) and water (40 mL). The mixture was stirred to obtain a clear solution. To the clear solution, ethyl acetate (100 mL) was added. While stirring, 3M HCl (3.2 mL) was added slowly until pH 1 was attained. The mixture was stirred for 10 minutes and organic layer was separated. The aqueous layer was extracted with ethyl acetate (2×100 mL). The combined organic layers was washed with water (2×100 mL), brine (1×50 mL) and dried over anhydrous Na2SO4. The ethyl acetate solution of treprostinil was filtered and the filtrate was concentrated under vacuum at 50° C. to give off-white solid. The crude treprostinil was recrystallized from 50% ethanol in water (70 mL). The pure treprostinil was collected in a Buchner funnel by filtration and cake was washed with cold 20% ethanolic solution in water. The cake of treprostinil was air-dried overnight and further dried in a vacuum oven at 50° C. under high vacuum to afford 2.9 g of treprostinil (Yield 91.4%, purity (HPLC, AUC, 99.8%).Analytical Data on Treprostinil from Treprostinil Diethanolamine Salt (1:1) to Treprostinil Batch No. Yield Purity (HPLC) 1 91.0% 99.8% (AUC) 2 92.0% 99.9% (AUC) 3 93.1% 99.7% (AUC) 4 93.3% 99.7% (AUC) 5 99.0% 99.8% (AUC) 6 94.6% 99.8% (AUC)

References:

UNITED THERAPEUTICS CORPORATION US2009/163738, 2009, A1 Location in patent:Page/Page column 7-8

1355990-07-6 Synthesis
Treprostinil Ethyl Ester

1355990-07-6
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