(4-but-2-ynyloxy-benzenesulfonyl)-(1-cyclopropanecarbonyl-piperidin-4-yl)-acetic acid ethyl ester

Base Information

Chemical Name:(4-but-2-ynyloxy-benzenesulfonyl)-(1-cyclopropanecarbonyl-piperidin-4-yl)-acetic acid ethyl ester
CAS No.:1026869-57-7
Molecular Formula:C₂₃H₂₉NO₆S
Molecular Weight:447.552
Hs Code.:

Synonyms:(4-but-2-ynyloxy-benzenesulfonyl)-(1-cyclopropanecarbonyl-piperidin-4-yl)-acetic acid ethyl ester

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Chemical Property of (4-but-2-ynyloxy-benzenesulfonyl)-(1-cyclopropanecarbonyl-piperidin-4-yl)-acetic acid ethyl ester

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Technology Process of (4-but-2-ynyloxy-benzenesulfonyl)-(1-cyclopropanecarbonyl-piperidin-4-yl)-acetic acid ethyl ester

There total 4 articles about (4-but-2-ynyloxy-benzenesulfonyl)-(1-cyclopropanecarbonyl-piperidin-4-yl)-acetic acid ethyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 4023-34-1
cyclopropanecarboxylic acid chloride

: 287393-47-9
ethyl {[4-(2-butynyloxy)phenyl]sulfonyl}(4-piperidinyl)acetate

: 1026869-57-7
(4-but-2-ynyloxy-benzenesulfonyl)-(1-cyclopropanecarbonyl-piperidin-4-yl)-acetic acid ethyl ester

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃;
DOI:10.1021/jm040086x

Reference yield:

: 287202-47-5
4-but-2-ynyloxy-benzenesulfonyl fluoride

: 1026869-57-7
(4-but-2-ynyloxy-benzenesulfonyl)-(1-cyclopropanecarbonyl-piperidin-4-yl)-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 46 percent / sodium bis(trimethylsilyl)amide / tetrahydrofuran / 1.5 h / -10 °C

2: HCl / ethanol / 20 °C

3: Et₃N / CH₂Cl₂ / 20 °C

With hydrogenchloride; sodium hexamethyldisilazane; triethylamine; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1021/jm040086x

Reference yield:

: 286459-94-7
4-but-2-ynyloxybenzenesulfonyl chloride

: 1026869-57-7
(4-but-2-ynyloxy-benzenesulfonyl)-(1-cyclopropanecarbonyl-piperidin-4-yl)-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 80 percent / KF; CaF₂ / acetonitrile / 4 h / 50 °C

2: 46 percent / sodium bis(trimethylsilyl)amide / tetrahydrofuran / 1.5 h / -10 °C

3: HCl / ethanol / 20 °C

4: Et₃N / CH₂Cl₂ / 20 °C

With hydrogenchloride; calcium fluoride; potassium fluoride; sodium hexamethyldisilazane; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; acetonitrile;
DOI:10.1021/jm040086x