(1S)-1-<(benzyloxycarbonyl)amino>-1-(benzyloxycarbonyl)-2-ethyl (2R)-1,2-bis(hexanoyloxy)-1-propyl phenyl phosphate

Base Information

Chemical Name:(1S)-1-<(benzyloxycarbonyl)amino>-1-(benzyloxycarbonyl)-2-ethyl (2R)-1,2-bis(hexanoyloxy)-1-propyl phenyl phosphate
CAS No.:161510-92-5
Molecular Formula:C₃₉H₅₀NO₁₂P
Molecular Weight:755.799
Hs Code.:

Synonyms:(1S)-1-<(benzyloxycarbonyl)amino>-1-(benzyloxycarbonyl)-2-ethyl (2R)-1,2-bis(hexanoyloxy)-1-propyl phenyl phosphate

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Chemical Property of (1S)-1-<(benzyloxycarbonyl)amino>-1-(benzyloxycarbonyl)-2-ethyl (2R)-1,2-bis(hexanoyloxy)-1-propyl phenyl phosphate

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Technology Process of (1S)-1-<(benzyloxycarbonyl)amino>-1-(benzyloxycarbonyl)-2-ethyl (2R)-1,2-bis(hexanoyloxy)-1-propyl phenyl phosphate

There total 6 articles about (1S)-1-<(benzyloxycarbonyl)amino>-1-(benzyloxycarbonyl)-2-ethyl (2R)-1,2-bis(hexanoyloxy)-1-propyl phenyl phosphate 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:

: 21209-51-8
N-benzyloxycarbonyl-L-serine benzyl ester

: 161510-92-5
(1S)-1-<(benzyloxycarbonyl)amino>-1-(benzyloxycarbonyl)-2-ethyl (2R)-1,2-bis(hexanoyloxy)-1-propyl phenyl phosphate

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) N,N-diisopropylethylamine / 1.) THF, -78 deg C, 15 min, 2.) THF, a) -78 deg C, 1 h, b) 25 deg C, 14 h

2: 30percent H₂O₂ / CH₂Cl₂

With dihydrogen peroxide; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1021/jm00050a009

Reference yield:

: 142-61-0
Hexanoyl chloride

: 161510-92-5
(1S)-1-<(benzyloxycarbonyl)amino>-1-(benzyloxycarbonyl)-2-ethyl (2R)-1,2-bis(hexanoyloxy)-1-propyl phenyl phosphate

Guidance literature:: Multi-step reaction with 4 steps

1: 84 percent / Et₃N, 4-(dimethylamino)pyridine / CH₂Cl₂ / 6 h / 25 °C

2: 85 percent / AcOH, H₂ / 10percent Pd/C / propan-2-ol / 18 h / 2585.7 Torr

3: 1.) N,N-diisopropylethylamine / 1.) THF, -78 deg C, 15 min, 2.) THF, a) -78 deg C, 1 h, b) 25 deg C, 14 h

4: 30percent H₂O₂ / CH₂Cl₂

With dmap; hydrogen; dihydrogen peroxide; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In dichloromethane; isopropyl alcohol;
DOI:10.1021/jm00050a009

Reference yield:

: 108609-67-2
benzyl (2S)-2,3-bis(hexanoyloxy)-1-propyl ether

: 161510-92-5
(1S)-1-<(benzyloxycarbonyl)amino>-1-(benzyloxycarbonyl)-2-ethyl (2R)-1,2-bis(hexanoyloxy)-1-propyl phenyl phosphate

Guidance literature:: Multi-step reaction with 3 steps

1: 85 percent / AcOH, H₂ / 10percent Pd/C / propan-2-ol / 18 h / 2585.7 Torr

2: 1.) N,N-diisopropylethylamine / 1.) THF, -78 deg C, 15 min, 2.) THF, a) -78 deg C, 1 h, b) 25 deg C, 14 h

3: 30percent H₂O₂ / CH₂Cl₂

With hydrogen; dihydrogen peroxide; acetic acid; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In dichloromethane; isopropyl alcohol;
DOI:10.1021/jm00050a009