(2R,3R)-3-Methyl-oxirane-2-carboxylic acid benzenesulfonylmethyl-(3,4-dimethoxy-phenyl)-amide

Base Information

Chemical Name:(2R,3R)-3-Methyl-oxirane-2-carboxylic acid benzenesulfonylmethyl-(3,4-dimethoxy-phenyl)-amide
CAS No.:84939-39-9
Molecular Formula:C₁₉H₂₁NO₆S
Molecular Weight:391.445
Hs Code.:

Synonyms:(2R,3R)-3-Methyl-oxirane-2-carboxylic acid benzenesulfonylmethyl-(3,4-dimethoxy-phenyl)-amide

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Chemical Property of (2R,3R)-3-Methyl-oxirane-2-carboxylic acid benzenesulfonylmethyl-(3,4-dimethoxy-phenyl)-amide

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Technology Process of (2R,3R)-3-Methyl-oxirane-2-carboxylic acid benzenesulfonylmethyl-(3,4-dimethoxy-phenyl)-amide

There total 5 articles about (2R,3R)-3-Methyl-oxirane-2-carboxylic acid benzenesulfonylmethyl-(3,4-dimethoxy-phenyl)-amide 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:

: 7205-91-6
phenylthiomethyl chloride

: 84939-39-9
(2R,3R)-3-Methyl-oxirane-2-carboxylic acid benzenesulfonylmethyl-(3,4-dimethoxy-phenyl)-amide

Guidance literature:: Multi-step reaction with 2 steps

1: 50percent aq. NaOH / benzyltriethylammonium iodide / CH₂Cl₂ / 1 h / Ambient temperature

2: m-chloroperbenzoic acid / CH₂Cl₂ / 16 h / Ambient temperature

With sodium hydroxide; 3-chloro-benzenecarboperoxoic acid; triethylbenzylammonium iodide; In dichloromethane;
DOI:10.1016/S0040-4039(00)81597-X

Reference yield:

: 84939-35-5
(2R,3R)-3-Methyl-oxirane-2-carboxylic acid (3,4-dimethoxy-phenyl)-amide

: 84939-39-9
(2R,3R)-3-Methyl-oxirane-2-carboxylic acid benzenesulfonylmethyl-(3,4-dimethoxy-phenyl)-amide

Guidance literature:: Multi-step reaction with 2 steps

1: 50percent aq. NaOH / benzyltriethylammonium iodide / CH₂Cl₂ / 1 h / Ambient temperature

2: m-chloroperbenzoic acid / CH₂Cl₂ / 16 h / Ambient temperature

With sodium hydroxide; 3-chloro-benzenecarboperoxoic acid; triethylbenzylammonium iodide; In dichloromethane;
DOI:10.1016/S0040-4039(00)81597-X

Reference yield:

: 84939-31-1
(2S,3R)-2-Bromo-N-(3,4-dimethoxy-phenyl)-3-hydroxy-butyramide

: 84939-39-9
(2R,3R)-3-Methyl-oxirane-2-carboxylic acid benzenesulfonylmethyl-(3,4-dimethoxy-phenyl)-amide

Guidance literature:: Multi-step reaction with 3 steps

1: 50percent aq NaOH / benzyltriethylammonium iodide / CH₂Cl₂ / 0.5 h / Ambient temperature

2: 50percent aq. NaOH / benzyltriethylammonium iodide / CH₂Cl₂ / 1 h / Ambient temperature

3: m-chloroperbenzoic acid / CH₂Cl₂ / 16 h / Ambient temperature

With sodium hydroxide; 3-chloro-benzenecarboperoxoic acid; triethylbenzylammonium iodide; In dichloromethane;
DOI:10.1016/S0040-4039(00)81597-X