(4R,5S)-3-benzoyl-5-hydroxy-N-methoxy-2,2-dimethylthiazolidine-4-carboxamide

Base Information

Chemical Name:(4R,5S)-3-benzoyl-5-hydroxy-N-methoxy-2,2-dimethylthiazolidine-4-carboxamide
CAS No.:1334521-38-8
Molecular Formula:C₁₄H₁₈N₂O₄S
Molecular Weight:310.374
Hs Code.:

Synonyms:(4R,5S)-3-benzoyl-5-hydroxy-N-methoxy-2,2-dimethylthiazolidine-4-carboxamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (4R,5S)-3-benzoyl-5-hydroxy-N-methoxy-2,2-dimethylthiazolidine-4-carboxamide

Chemical Property:

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Technology Process of (4R,5S)-3-benzoyl-5-hydroxy-N-methoxy-2,2-dimethylthiazolidine-4-carboxamide

There total 4 articles about (4R,5S)-3-benzoyl-5-hydroxy-N-methoxy-2,2-dimethylthiazolidine-4-carboxamide 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:

: C₁₄H₁₈N₂O₅S

: 1334521-38-8
(4R,5S)-3-benzoyl-5-hydroxy-N-methoxy-2,2-dimethylthiazolidine-4-carboxamide

Guidance literature:: With dimethylsulfide; In tetrahydrofuran; at 20 ℃;
DOI:10.1016/j.tetlet.2011.07.085

Reference yield:

: 1334521-36-6
(R)-3-benzoyl-N-methoxy-2,2-dimethylthiazolidine-4-carboxamide

: 1334521-38-8
(4R,5S)-3-benzoyl-5-hydroxy-N-methoxy-2,2-dimethylthiazolidine-4-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: oxygen / tetrahydrofuran / -10 - 0 °C / UV-irradiation

2: dimethylsulfide / tetrahydrofuran / 20 °C

With dimethylsulfide; oxygen; In tetrahydrofuran; 1: Pummerer type rearrangement;
DOI:10.1016/j.tetlet.2011.07.085

Reference yield:

: C₁₈H₂₃NO₅S

: 1334521-38-8
(4R,5S)-3-benzoyl-5-hydroxy-N-methoxy-2,2-dimethylthiazolidine-4-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: -20 °C

2: oxygen / tetrahydrofuran / -10 - 0 °C / UV-irradiation

3: dimethylsulfide / tetrahydrofuran / 20 °C

With dimethylsulfide; oxygen; In tetrahydrofuran; 2: Pummerer type rearrangement;
DOI:10.1016/j.tetlet.2011.07.085