(2R,3R)-1-[4-(4-Chloro-2-fluoro-benzyloxy)-benzenesulfonyl]-3-hydroxy-3-methyl-piperidine-2-carboxylic acid

Base Information

Chemical Name:(2R,3R)-1-[4-(4-Chloro-2-fluoro-benzyloxy)-benzenesulfonyl]-3-hydroxy-3-methyl-piperidine-2-carboxylic acid
CAS No.:862540-08-7
Molecular Formula:C₂₀H₂₁ClFNO₆S
Molecular Weight:457.907
Hs Code.:

Synonyms:(2R,3R)-1-[4-(4-Chloro-2-fluoro-benzyloxy)-benzenesulfonyl]-3-hydroxy-3-methyl-piperidine-2-carboxylic acid

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Chemical Property of (2R,3R)-1-[4-(4-Chloro-2-fluoro-benzyloxy)-benzenesulfonyl]-3-hydroxy-3-methyl-piperidine-2-carboxylic acid

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Technology Process of (2R,3R)-1-[4-(4-Chloro-2-fluoro-benzyloxy)-benzenesulfonyl]-3-hydroxy-3-methyl-piperidine-2-carboxylic acid

There total 3 articles about (2R,3R)-1-[4-(4-Chloro-2-fluoro-benzyloxy)-benzenesulfonyl]-3-hydroxy-3-methyl-piperidine-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: 100.0%

: 950889-28-8
(2R,3R)-1-[4-(4-Chloro-2-fluoro-benzyloxy)-benzenesulfonyl]-3-hydroxy-3-methyl-piperidine-2-carboxylic acid tert-butyl ester

: 862540-08-7
(2R,3R)-1-[4-(4-Chloro-2-fluoro-benzyloxy)-benzenesulfonyl]-3-hydroxy-3-methyl-piperidine-2-carboxylic acid

Guidance literature:: With trifluoroacetic acid; In dichloromethane;
DOI:10.1016/j.bmcl.2005.05.037

Reference yield:

: 915694-06-3
(2R,3R)-1-(4-Benzyloxy-benzenesulfonyl)-3-hydroxy-3-methyl-piperidine-2-carboxylic acid tert-butyl ester

: 862540-08-7
(2R,3R)-1-[4-(4-Chloro-2-fluoro-benzyloxy)-benzenesulfonyl]-3-hydroxy-3-methyl-piperidine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / H₂ / Pd/C / methanol

2: 80 percent / Cs₂CO₃ / dimethylformamide

3: 100 percent / TFA / CH₂Cl₂

With hydrogen; caesium carbonate; trifluoroacetic acid; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2005.05.037

Reference yield:

: 862539-71-7
(2R,3R)-3-Hydroxy-1-(4-hydroxy-benzenesulfonyl)-3-methyl-piperidine-2-carboxylic acid tert-butyl ester

: 862540-08-7
(2R,3R)-1-[4-(4-Chloro-2-fluoro-benzyloxy)-benzenesulfonyl]-3-hydroxy-3-methyl-piperidine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / Cs₂CO₃ / dimethylformamide

2: 100 percent / TFA / CH₂Cl₂

With caesium carbonate; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2005.05.037