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ChemicalBook CAS DataBase List 2-thienyl)-3-butenyl]-, ethyl ester, (3R)-

2-thienyl)-3-butenyl]-, ethyl ester, (3R)- synthesis

9synthesis methods
4,4-bis(3-methylthiophen-2-yl)but-3-en-1-yl methanesulfonate

847233-13-0
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25137-01-3 Synthesis
Ethyl (3R)-piperidine-3-carboxylate

25137-01-3
263 suppliers
$9.00/1g

2-thienyl)-3-butenyl]-, ethyl ester, (3R)-

145821-58-5
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Yield:145821-58-5 75.5%

Reaction Conditions:

with potassium carbonate;potassium iodide in acetone at 20; for 72 h;

Steps:

11 Preparation and Purification of tiagabine hydrochloride: Example 11--through(RThe reaction piperidine-3-carboxylic acid ethyl ester and 1,1-bis (3-methyl-2-thienyl) -1-butene 4-sulfonate -)

At room temperature R-piperidine-3-carboxylate 62.0g (395mmol), 1,1-bis(3-methyl-2-thienyl)-4-methyl-1-butene sulfonate 133g (395mmol), anhydrous K2CO3 200g (1.45mol), the mixture was stirred 3L and acetone KI 3.5g 72 hours, inorganic salts were removed by filtration, the filtrate was rotary evaporated to a red oil.

References:

CN103570703,2016,B Location in patent:Paragraph 0073; 0074