(2R)-2-methyl-1-(4-(1,1,1-trifluoro-2-hydroxypropan-2-yl)phenylsulfonyl)pyrrolidine-2-carboxylic acid

Base Information

Chemical Name:(2R)-2-methyl-1-(4-(1,1,1-trifluoro-2-hydroxypropan-2-yl)phenylsulfonyl)pyrrolidine-2-carboxylic acid
CAS No.:1400280-22-9
Molecular Formula:C₁₅H₁₈F₃NO₅S
Molecular Weight:381.373
Hs Code.:

Synonyms:(2R)-2-methyl-1-(4-(1,1,1-trifluoro-2-hydroxypropan-2-yl)phenylsulfonyl)pyrrolidine-2-carboxylic acid

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Chemical Property of (2R)-2-methyl-1-(4-(1,1,1-trifluoro-2-hydroxypropan-2-yl)phenylsulfonyl)pyrrolidine-2-carboxylic acid

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Technology Process of (2R)-2-methyl-1-(4-(1,1,1-trifluoro-2-hydroxypropan-2-yl)phenylsulfonyl)pyrrolidine-2-carboxylic acid

There total 3 articles about (2R)-2-methyl-1-(4-(1,1,1-trifluoro-2-hydroxypropan-2-yl)phenylsulfonyl)pyrrolidine-2-carboxylic acid 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: 50.0%

: C₁₆H₂₀F₃NO₅S

: 1400280-22-9
(2R)-2-methyl-1-(4-(1,1,1-trifluoro-2-hydroxypropan-2-yl)phenylsulfonyl)pyrrolidine-2-carboxylic acid

Guidance literature:: With water; sodium hydroxide; In tetrahydrofuran; methanol; at 20 ℃;
DOI:10.1021/ml300144n

Reference yield:

: 63399-77-9
(R)-2-Methyl-1-azacyclopentan-2-carbonsaeure

: 1400280-22-9
(2R)-2-methyl-1-(4-(1,1,1-trifluoro-2-hydroxypropan-2-yl)phenylsulfonyl)pyrrolidine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: thionyl chloride / Reflux; Inert atmosphere

2: triethylamine / dichloromethane / 2 h / 20 °C / Inert atmosphere

3: tetrabutyl ammonium fluoride / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

4: water; sodium hydroxide / tetrahydrofuran; methanol / 20 °C

With thionyl chloride; tetrabutyl ammonium fluoride; water; triethylamine; sodium hydroxide; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/ml300144n

Reference yield:

: 1788-10-9
4-Acetylbenzenesulfonyl chloride

: 1400280-22-9
(2R)-2-methyl-1-(4-(1,1,1-trifluoro-2-hydroxypropan-2-yl)phenylsulfonyl)pyrrolidine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / dichloromethane / 2 h / 20 °C / Inert atmosphere

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

3: water; sodium hydroxide / tetrahydrofuran; methanol / 20 °C

With tetrabutyl ammonium fluoride; water; triethylamine; sodium hydroxide; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/ml300144n