(R)-N-(2,2-dimethylpropyl)-3-{(2S,3S)-3-[(2S)-2-amino-3,3-dimethylbutanoylamino]-2-hydroxy-4-phenylbutanoyl}-5,5-dimethyl-1,3-thiazolidine-4-carboxamide

Base Information

Chemical Name:(R)-N-(2,2-dimethylpropyl)-3-{(2S,3S)-3-[(2S)-2-amino-3,3-dimethylbutanoylamino]-2-hydroxy-4-phenylbutanoyl}-5,5-dimethyl-1,3-thiazolidine-4-carboxamide
CAS No.:1061338-75-7
Molecular Formula:C₂₇H₄₄N₄O₄S
Molecular Weight:520.737
Hs Code.:

(R)-N-(2,2-dimethylpropyl)-3-{(2S,3S)-3-[(2S)-2-amino-3,3-dimethylbutanoylamino]-2-hydroxy-4-phenylbutanoyl}-5,5-dimethyl-1,3-thiazolidine-4-carboxamide

Synonyms:(R)-N-(2,2-dimethylpropyl)-3-{(2S,3S)-3-[(2S)-2-amino-3,3-dimethylbutanoylamino]-2-hydroxy-4-phenylbutanoyl}-5,5-dimethyl-1,3-thiazolidine-4-carboxamide

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Chemical Property of (R)-N-(2,2-dimethylpropyl)-3-{(2S,3S)-3-[(2S)-2-amino-3,3-dimethylbutanoylamino]-2-hydroxy-4-phenylbutanoyl}-5,5-dimethyl-1,3-thiazolidine-4-carboxamide

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Technology Process of (R)-N-(2,2-dimethylpropyl)-3-{(2S,3S)-3-[(2S)-2-amino-3,3-dimethylbutanoylamino]-2-hydroxy-4-phenylbutanoyl}-5,5-dimethyl-1,3-thiazolidine-4-carboxamide

There total 12 articles about (R)-N-(2,2-dimethylpropyl)-3-{(2S,3S)-3-[(2S)-2-amino-3,3-dimethylbutanoylamino]-2-hydroxy-4-phenylbutanoyl}-5,5-dimethyl-1,3-thiazolidine-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:

: C₃₂H₅₂N₄O₆S

: 1061338-75-7
(R)-N-(2,2-dimethylpropyl)-3-{(2S,3S)-3-[(2S)-2-amino-3,3-dimethylbutanoylamino]-2-hydroxy-4-phenylbutanoyl}-5,5-dimethyl-1,3-thiazolidine-4-carboxamide

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 1h;
DOI:10.1016/j.bmc.2008.05.052

Reference yield:

: 117918-23-7
(R)-3-tert-butoxycarbonyl-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid

: 1061338-75-7
(R)-N-(2,2-dimethylpropyl)-3-{(2S,3S)-3-[(2S)-2-amino-3,3-dimethylbutanoylamino]-2-hydroxy-4-phenylbutanoyl}-5,5-dimethyl-1,3-thiazolidine-4-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1: (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine / N,N-dimethyl-formamide / 20 °C

2: hydrogenchloride / 1,4-dioxane / 0.5 h / 20 °C

3: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 0.5 h / 20 °C

4: hydrogenchloride / 1,4-dioxane / 0.5 h / 20 °C

5: (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine / N,N-dimethyl-formamide / 20 °C

6: hydrogenchloride / 1,4-dioxane / 0.5 h / 20 °C

With hydrogenchloride; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.01.048

Reference yield:

: 1061338-51-9
(R)-N-(2,2-dimethylpropyl)-5,5-dimethyl-1,3-thiazolidine-4-carboxamide

: 1061338-75-7
(R)-N-(2,2-dimethylpropyl)-3-{(2S,3S)-3-[(2S)-2-amino-3,3-dimethylbutanoylamino]-2-hydroxy-4-phenylbutanoyl}-5,5-dimethyl-1,3-thiazolidine-4-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 0.5 h / 20 °C

2: hydrogenchloride / 1,4-dioxane / 0.5 h / 20 °C

3: (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine / N,N-dimethyl-formamide / 20 °C

4: hydrogenchloride / 1,4-dioxane / 0.5 h / 20 °C

With hydrogenchloride; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.01.048