(4S)-1-benzyl-3-<(2S)-2-amino>propionyl>-2-oxoimidazolidine-4-carboxylic acid

Base Information

Chemical Name:(4S)-1-benzyl-3-<(2S)-2-amino>propionyl>-2-oxoimidazolidine-4-carboxylic acid
CAS No.:89371-56-2
Molecular Formula:C₃₁H₃₃N₃O₆
Molecular Weight:543.62
Hs Code.:

(4S)-1-benzyl-3-<(2S)-2-<N-<(1S)-1-(benzyloxycarbonyl)-3-phenylpropyl>amino>propionyl>-2-oxoimidazolidine-4-carboxylic acid

Synonyms:(4S)-1-benzyl-3-<(2S)-2-amino>propionyl>-2-oxoimidazolidine-4-carboxylic acid

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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 (4S)-1-benzyl-3-<(2S)-2-amino>propionyl>-2-oxoimidazolidine-4-carboxylic acid

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Technology Process of (4S)-1-benzyl-3-<(2S)-2-amino>propionyl>-2-oxoimidazolidine-4-carboxylic acid

There total 5 articles about (4S)-1-benzyl-3-<(2S)-2-amino>propionyl>-2-oxoimidazolidine-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: 91.9%

: hydrogen chloride-dioxane

: 89371-55-1
tert-butyl (4S)-1-benzyl-3-<(2S)-2-amino>propionyl>-2-oxoimidazolidine-4-carboxylate

: 89371-56-2
(4S)-1-benzyl-3-<(2S)-2-amino>propionyl>-2-oxoimidazolidine-4-carboxylic acid

Guidance literature:: In water; ethyl acetate;

Reference yield:

: 83057-00-5
(S)-3-benzyl-2-oxo-imidazolidine-1,5-dicarboxylic acid 1-benzyl ester 5-t-butyl ester

: 89371-56-2
(4S)-1-benzyl-3-<(2S)-2-amino>propionyl>-2-oxoimidazolidine-4-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 94.3 percent / H₂ / Pd / methanol / 3 h / 760 Torr / Ambient temperature

2: 1) KOtBu / 1) THF, -50 deg C, 20 min, 2) -30 deg C, 1 h

3: 10.1 percent / K₂CO₃ / hexamethylphosphoric acid triamide / 48 h / Ambient temperature

4: 1 g / 15percent HCl/dioxane / Ambient temperature

With hydrogenchloride; potassium tert-butylate; hydrogen; potassium carbonate; palladium; In methanol; N,N,N,N,N,N-hexamethylphosphoric triamide;
DOI:10.1021/jm00122a003

Reference yield:

: 83057-01-6
tert.-butyl (4S)-1-benzyl-2-oxo-imidazolidine-4-carboxylate

: 89371-56-2
(4S)-1-benzyl-3-<(2S)-2-amino>propionyl>-2-oxoimidazolidine-4-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 1) KOtBu / 1) THF, -50 deg C, 20 min, 2) -30 deg C, 1 h

2: 10.1 percent / K₂CO₃ / hexamethylphosphoric acid triamide / 48 h / Ambient temperature

3: 1 g / 15percent HCl/dioxane / Ambient temperature

With hydrogenchloride; potassium tert-butylate; potassium carbonate; In N,N,N,N,N,N-hexamethylphosphoric triamide;
DOI:10.1021/jm00122a003