6-[(S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-2-phenyl-acetylamino]-hexanoic acid (S)-2-((R)-3,4-bis-benzyloxy-5-oxo-2,5-dihydro-furan-2-yl)-2-hydroxy-ethyl ester

Base Information

Chemical Name:6-[(S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-2-phenyl-acetylamino]-hexanoic acid (S)-2-((R)-3,4-bis-benzyloxy-5-oxo-2,5-dihydro-furan-2-yl)-2-hydroxy-ethyl ester
CAS No.:867022-09-1
Molecular Formula:C₄₂H₅₁N₃O₁₁
Molecular Weight:773.88
Hs Code.:

6-[(S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-2-phenyl-acetylamino]-hexanoic acid (S)-2-((R)-3,4-bis-benzyloxy-5-oxo-2,5-dihydro-furan-2-yl)-2-hydroxy-ethyl ester

Synonyms:6-[(S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-2-phenyl-acetylamino]-hexanoic acid (S)-2-((R)-3,4-bis-benzyloxy-5-oxo-2,5-dihydro-furan-2-yl)-2-hydroxy-ethyl ester

Suppliers and Price of 6-[(S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-2-phenyl-acetylamino]-hexanoic acid (S)-2-((R)-3,4-bis-benzyloxy-5-oxo-2,5-dihydro-furan-2-yl)-2-hydroxy-ethyl ester

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 6-[(S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-2-phenyl-acetylamino]-hexanoic acid (S)-2-((R)-3,4-bis-benzyloxy-5-oxo-2,5-dihydro-furan-2-yl)-2-hydroxy-ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 6-[(S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-2-phenyl-acetylamino]-hexanoic acid (S)-2-((R)-3,4-bis-benzyloxy-5-oxo-2,5-dihydro-furan-2-yl)-2-hydroxy-ethyl ester

There total 5 articles about 6-[(S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-2-phenyl-acetylamino]-hexanoic acid (S)-2-((R)-3,4-bis-benzyloxy-5-oxo-2,5-dihydro-furan-2-yl)-2-hydroxy-ethyl ester 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: 60.0%

: 867021-96-3
N-[N-(tert-butyloxycarbonyl)-L-alanyl]-(2S)-2-phenylglycine

: 6-O-(6-aminocaproyl)-2,3-di-O-benzyl-L-ascorbic acid trifluoroacetic salt

: 867022-09-1
6-[(S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-2-phenyl-acetylamino]-hexanoic acid (S)-2-((R)-3,4-bis-benzyloxy-5-oxo-2,5-dihydro-furan-2-yl)-2-hydroxy-ethyl ester

Guidance literature:: With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20 ℃;
DOI:10.1071/CH05102

Reference yield:

: tert-butyl (S)-2-amino-2-phenylacetate hydrochloride

: 867022-09-1
6-[(S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-2-phenyl-acetylamino]-hexanoic acid (S)-2-((R)-3,4-bis-benzyloxy-5-oxo-2,5-dihydro-furan-2-yl)-2-hydroxy-ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 3.70 g / BOP; ethyldiisopropylamine / CH₂Cl₂ / 20 °C

2: 96 percent / H₂ / Pd(OH)2 on activated charcoal / methanol / 20 °C

3: 2.30 g / CH₂Cl₂ / 20 °C

4: 80 percent / ethyldiisopropylamine / CH₂Cl₂ / 20 °C

5: 60 percent / BOP; ethyldiisopropylamine / CH₂Cl₂ / 0 - 20 °C

With hydrogen; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; palladium hydroxide - carbon; In methanol; dichloromethane;
DOI:10.1071/CH05102

Reference yield:

: 860013-16-7
N-(N-carbobenzyloxy-L-alanyl)-(2S)-2-phenylglycine tert-butyl ester

: 867022-09-1
6-[(S)-2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-2-phenyl-acetylamino]-hexanoic acid (S)-2-((R)-3,4-bis-benzyloxy-5-oxo-2,5-dihydro-furan-2-yl)-2-hydroxy-ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 96 percent / H₂ / Pd(OH)2 on activated charcoal / methanol / 20 °C

2: 2.30 g / CH₂Cl₂ / 20 °C

3: 80 percent / ethyldiisopropylamine / CH₂Cl₂ / 20 °C

4: 60 percent / BOP; ethyldiisopropylamine / CH₂Cl₂ / 0 - 20 °C

With hydrogen; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; palladium hydroxide - carbon; In methanol; dichloromethane;
DOI:10.1071/CH05102