(2S,3R)-3-[((S)-1-Methoxycarbonyl-ethylamino)-methyl]-2-(9-phenyl-9H-fluoren-9-ylamino)-pentanoic acid methyl ester

Base Information

Chemical Name:(2S,3R)-3-[((S)-1-Methoxycarbonyl-ethylamino)-methyl]-2-(9-phenyl-9H-fluoren-9-ylamino)-pentanoic acid methyl ester
CAS No.:120230-75-3
Molecular Formula:C₃₀H₃₄N₂O₄
Molecular Weight:486.611
Hs Code.:

Synonyms:(2S,3R)-3-[((S)-1-Methoxycarbonyl-ethylamino)-methyl]-2-(9-phenyl-9H-fluoren-9-ylamino)-pentanoic acid methyl ester

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Chemical Property of (2S,3R)-3-[((S)-1-Methoxycarbonyl-ethylamino)-methyl]-2-(9-phenyl-9H-fluoren-9-ylamino)-pentanoic acid methyl ester

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Technology Process of (2S,3R)-3-[((S)-1-Methoxycarbonyl-ethylamino)-methyl]-2-(9-phenyl-9H-fluoren-9-ylamino)-pentanoic acid methyl ester

There total 4 articles about (2S,3R)-3-[((S)-1-Methoxycarbonyl-ethylamino)-methyl]-2-(9-phenyl-9H-fluoren-9-ylamino)-pentanoic acid methyl 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: 64.0%

: 2491-20-5
L-alanine methyl ester hydrochloride

: 120230-73-1
methyl (2S,3S)-2-<(9-phenylfluorenyl)amino>-3-ethyl-4-oxobutanoate

: 120230-75-3
(2S,3R)-3-[((S)-1-Methoxycarbonyl-ethylamino)-methyl]-2-(9-phenyl-9H-fluoren-9-ylamino)-pentanoic acid methyl ester

Guidance literature:: With sodium cyanoborohydride; In methanol; for 3h; Ambient temperature;
DOI:10.1021/jo00274a037

Reference yield:

: 120230-62-8
dimethyl (S)-N-(9-phenyl-9H-fluoren-9-yl)aspartate

: 120230-75-3
(2S,3R)-3-[((S)-1-Methoxycarbonyl-ethylamino)-methyl]-2-(9-phenyl-9H-fluoren-9-ylamino)-pentanoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) potassium hexamethyldisilazide (KHMDS) / 1.) THF, toluene, -75 deg C, 45 min, 2.) -75 deg C, 10 min

2: diisobutylaluminum hydride (DIBAL) / toluene; hexane / 0.33 h / -47 °C

3: N-chlorosuccinimide (NCS), (CH₃)2S / toluene / 4 h / -25 °C

4: 64 percent / NaCNBH₃ / methanol / 3 h / Ambient temperature

With N-chloro-succinimide; dimethylsulfide; potassium hexamethylsilazane; diisobutylaluminium hydride; sodium cyanoborohydride; In methanol; hexane; toluene;
DOI:10.1021/jo00274a037

Reference yield:

: 120230-70-8
methyl (2S,3S)-2-<(9-phenylfluorenyl)amino>-3-ethyl-4-hydroxybutanoate

: 120230-75-3
(2S,3R)-3-[((S)-1-Methoxycarbonyl-ethylamino)-methyl]-2-(9-phenyl-9H-fluoren-9-ylamino)-pentanoic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: N-chlorosuccinimide (NCS), (CH₃)2S / toluene / 4 h / -25 °C

2: 64 percent / NaCNBH₃ / methanol / 3 h / Ambient temperature

With N-chloro-succinimide; dimethylsulfide; sodium cyanoborohydride; In methanol; toluene;
DOI:10.1021/jo00274a037