(2S,4R)-2-benzoyl-N-(prop-2-ynyloxyacetyl)thiazolidine-4-carboxylic acid

Base Information

Chemical Name:(2S,4R)-2-benzoyl-N-(prop-2-ynyloxyacetyl)thiazolidine-4-carboxylic acid
CAS No.:443683-51-0
Molecular Formula:C₁₆H₁₅NO₅S
Molecular Weight:333.365
Hs Code.:

Synonyms:(2S,4R)-2-benzoyl-N-(prop-2-ynyloxyacetyl)thiazolidine-4-carboxylic acid

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Chemical Property of (2S,4R)-2-benzoyl-N-(prop-2-ynyloxyacetyl)thiazolidine-4-carboxylic acid

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Technology Process of (2S,4R)-2-benzoyl-N-(prop-2-ynyloxyacetyl)thiazolidine-4-carboxylic acid

There total 5 articles about (2S,4R)-2-benzoyl-N-(prop-2-ynyloxyacetyl)thiazolidine-4-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: 95.0%

: 443683-45-2
methyl (2R,4R)-2-benzoyl-N-(prop-2-ynyloxyacetyl)thiazolidine-4-carboxylate

: 443683-51-0
(2S,4R)-2-benzoyl-N-(prop-2-ynyloxyacetyl)thiazolidine-4-carboxylic acid

Guidance literature:: methyl (2R,4R)-2-benzoyl-N-(prop-2-ynyloxyacetyl)thiazolidine-4-carboxylate; With lithium iodide; In ethyl acetate; for 6h; Heating;

With hydrogenchloride; In water; Further stages.;
DOI:10.1021/jo010807p

Reference yield:

: 1074-12-0
phenylglyoxal hydrate

: 443683-51-0
(2S,4R)-2-benzoyl-N-(prop-2-ynyloxyacetyl)thiazolidine-4-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium hydrogen carbonate / ethanol / 20 °C

2.1: 41 percent / anhydrous potassium carbonate / CH₂Cl₂ / 18 h / 20 °C

3.1: LiI / ethyl acetate / 6 h / Heating

3.2: 95 percent / HCl / H₂O

With potassium carbonate; potassium hydrogencarbonate; lithium iodide; In ethanol; dichloromethane; ethyl acetate;
DOI:10.1021/jo010807p

Reference yield:

: 77378-24-6
(prop-2-ynyloxy)acetic acid chloride

: 443683-51-0
(2S,4R)-2-benzoyl-N-(prop-2-ynyloxyacetyl)thiazolidine-4-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: 41 percent / anhydrous potassium carbonate / CH₂Cl₂ / 18 h / 20 °C

2.1: LiI / ethyl acetate / 6 h / Heating

2.2: 95 percent / HCl / H₂O

With potassium carbonate; lithium iodide; In dichloromethane; ethyl acetate;
DOI:10.1021/jo010807p