(2R,3R,4R,5S)-6-cyclohexyl-2-(cyclohexylmethyl)-3,4-dihydroxy-5-{[(2S)-3-(1H-imidazol-5-yl)-2-{[(naphthalen-1-yloxy)acetyl]amino}propanoyl]amino}-N-{(2S,3S)-3-methyl-1-oxo-1-[(pyridin-2-ylmethyl)amino]pentan-2-yl}hexanamide (non-preferred name)

Base Information

Chemical Name:(2R,3R,4R,5S)-6-cyclohexyl-2-(cyclohexylmethyl)-3,4-dihydroxy-5-{[(2S)-3-(1H-imidazol-5-yl)-2-{[(naphthalen-1-yloxy)acetyl]amino}propanoyl]amino}-N-{(2S,3S)-3-methyl-1-oxo-1-[(pyridin-2-ylmethyl)amino]pentan-2-yl}hexanamide (non-preferred name)
CAS No.:134458-75-6
Molecular Formula:C₄₉H₆₇N₇O₇
Molecular Weight:866.114
Hs Code.:

(2R,3R,4R,5S)-6-cyclohexyl-2-(cyclohexylmethyl)-3,4-dihydroxy-5-{[(2S)-3-(1H-imidazol-5-yl)-2-{[(naphthalen-1-yloxy)acetyl]amino}propanoyl]amino}-N-{(2S,3S)-3-methyl-1-oxo-1-[(pyridin-2-ylmethyl)amino]pentan-2-yl}hexanamide (non-preferred name)

Synonyms:

Suppliers and Price of (2R,3R,4R,5S)-6-cyclohexyl-2-(cyclohexylmethyl)-3,4-dihydroxy-5-{[(2S)-3-(1H-imidazol-5-yl)-2-{[(naphthalen-1-yloxy)acetyl]amino}propanoyl]amino}-N-{(2S,3S)-3-methyl-1-oxo-1-[(pyridin-2-ylmethyl)amino]pentan-2-yl}hexanamide (non-preferred name)

Supply Marketing:

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

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Total 1 raw suppliers

Chemical Property of (2R,3R,4R,5S)-6-cyclohexyl-2-(cyclohexylmethyl)-3,4-dihydroxy-5-{[(2S)-3-(1H-imidazol-5-yl)-2-{[(naphthalen-1-yloxy)acetyl]amino}propanoyl]amino}-N-{(2S,3S)-3-methyl-1-oxo-1-[(pyridin-2-ylmethyl)amino]pentan-2-yl}hexanamide (non-preferred name)

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:1188.9°Cat760mmHg
Flash Point:672.8°C
Density:1.207g/cm³

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of (2R,3R,4R,5S)-6-cyclohexyl-2-(cyclohexylmethyl)-3,4-dihydroxy-5-{[(2S)-3-(1H-imidazol-5-yl)-2-{[(naphthalen-1-yloxy)acetyl]amino}propanoyl]amino}-N-{(2S,3S)-3-methyl-1-oxo-1-[(pyridin-2-ylmethyl)amino]pentan-2-yl}hexanamide (non-preferred name)

There total 8 articles about (2R,3R,4R,5S)-6-cyclohexyl-2-(cyclohexylmethyl)-3,4-dihydroxy-5-{[(2S)-3-(1H-imidazol-5-yl)-2-{[(naphthalen-1-yloxy)acetyl]amino}propanoyl]amino}-N-{(2S,3S)-3-methyl-1-oxo-1-[(pyridin-2-ylmethyl)amino]pentan-2-yl}hexanamide (non-preferred name) 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:

: 4-{(S)-2-((1S,2R,3R,4R)-5-Cyclohexyl-1-cyclohexylmethyl-2,3-dihydroxy-4-{(1S,2S)-2-methyl-1-[(pyridin-2-ylmethyl)-carbamoyl]-butylcarbamoyl}-pentylcarbamoyl)-2-[2-(naphthalen-1-yloxy)-acetylamino]-ethyl}-imidazole-1-carboxylic acid tert-butyl ester

: 134458-75-6
(2R,3R,4R,5S)-6-Cyclohexyl-2-cyclohexylmethyl-3,4-dihydroxy-5-{(S)-3-(1H-imidazol-4-yl)-2-[2-(naphthalen-1-yloxy)-acetylamino]-propionylamino}-hexanoic acid {(1S,2S)-2-methyl-1-[(pyridin-2-ylmethyl)-carbamoyl]-butyl}-amide

Guidance literature:: With trifluoroacetic acid; In dichloromethane; for 0.25h;
DOI:10.1021/jm00112a005

Reference yield:

: 117997-58-7
tert-butyl (4S,5R)-4-(cyclohexylmethyl)-5-formyl-2,2-dimethyl-3-oxazolidinecarboxylate

: 134458-75-6
(2R,3R,4R,5S)-6-Cyclohexyl-2-cyclohexylmethyl-3,4-dihydroxy-5-{(S)-3-(1H-imidazol-4-yl)-2-[2-(naphthalen-1-yloxy)-acetylamino]-propionylamino}-hexanoic acid {(1S,2S)-2-methyl-1-[(pyridin-2-ylmethyl)-carbamoyl]-butyl}-amide

Guidance literature:: Multi-step reaction with 7 steps

2: aq. hydrogen peroxide, aq. lithium hydroxide / methanol / 4 h / Ambient temperature

3: 1.) camphorsulfonic acid, 2.) acetone / 1.) CH₂Cl₂, RT, 45 min, 2.) CH₂Cl₂, RT, 14 h

4: diisopropylethylamine, diethylphosphoryl cyanide / CH₂Cl₂ / 14 h / Ambient temperature

5: acetyl chloride, ethanedithiol / methanol / 5 h

6: diisopropylethylamine, (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate / CH₂Cl₂ / 14 h

7: trifluoroacetic acid / CH₂Cl₂ / 0.25 h

With ethandithiol; lithium hydroxide; diethylphosphoryl cyanide; camphor-10-sulfonic acid; dihydrogen peroxide; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; acetyl chloride; acetone; trifluoroacetic acid; In methanol; dichloromethane;
DOI:10.1021/jm00112a005

Reference yield:

: 134458-53-0
(4R,5S)-3-(3-Cyclohexyl-propionyl)-4-methyl-5-phenyl-oxazolidin-2-one

: 134458-75-6
(2R,3R,4R,5S)-6-Cyclohexyl-2-cyclohexylmethyl-3,4-dihydroxy-5-{(S)-3-(1H-imidazol-4-yl)-2-[2-(naphthalen-1-yloxy)-acetylamino]-propionylamino}-hexanoic acid {(1S,2S)-2-methyl-1-[(pyridin-2-ylmethyl)-carbamoyl]-butyl}-amide

Guidance literature:: Multi-step reaction with 7 steps

2: aq. hydrogen peroxide, aq. lithium hydroxide / methanol / 4 h / Ambient temperature

3: 1.) camphorsulfonic acid, 2.) acetone / 1.) CH₂Cl₂, RT, 45 min, 2.) CH₂Cl₂, RT, 14 h

4: diisopropylethylamine, diethylphosphoryl cyanide / CH₂Cl₂ / 14 h / Ambient temperature

5: acetyl chloride, ethanedithiol / methanol / 5 h

6: diisopropylethylamine, (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate / CH₂Cl₂ / 14 h

7: trifluoroacetic acid / CH₂Cl₂ / 0.25 h

With ethandithiol; lithium hydroxide; diethylphosphoryl cyanide; camphor-10-sulfonic acid; dihydrogen peroxide; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; acetyl chloride; acetone; trifluoroacetic acid; In methanol; dichloromethane;
DOI:10.1021/jm00112a005