[1-((R)-3-{(S)-1-((1S,2R,3S)-1-Cyclohexylmethyl-2,3-dihydroxy-5-pyridin-2-yl-pentylcarbamoyl)-2-[1-(2,4-dinitro-phenyl)-1H-imidazol-4-yl]-ethylcarbamoyl}-4-naphthalen-1-yl-butyryl)-piperidin-4-yl]-carbamic acid tert-butyl ester

Base Information

Chemical Name:[1-((R)-3-{(S)-1-((1S,2R,3S)-1-Cyclohexylmethyl-2,3-dihydroxy-5-pyridin-2-yl-pentylcarbamoyl)-2-[1-(2,4-dinitro-phenyl)-1H-imidazol-4-yl]-ethylcarbamoyl}-4-naphthalen-1-yl-butyryl)-piperidin-4-yl]-carbamic acid tert-butyl ester
CAS No.:135650-90-7
Molecular Formula:C₅₄H₆₇N₉O₁₁
Molecular Weight:1018.18
Hs Code.:

[1-((R)-3-{(S)-1-((1S,2R,3S)-1-Cyclohexylmethyl-2,3-dihydroxy-5-pyridin-2-yl-pentylcarbamoyl)-2-[1-(2,4-dinitro-phenyl)-1H-imidazol-4-yl]-ethylcarbamoyl}-4-naphthalen-1-yl-butyryl)-piperidin-4-yl]-carbamic acid tert-butyl ester

Synonyms:[1-((R)-3-{(S)-1-((1S,2R,3S)-1-Cyclohexylmethyl-2,3-dihydroxy-5-pyridin-2-yl-pentylcarbamoyl)-2-[1-(2,4-dinitro-phenyl)-1H-imidazol-4-yl]-ethylcarbamoyl}-4-naphthalen-1-yl-butyryl)-piperidin-4-yl]-carbamic acid tert-butyl ester

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Chemical Property of [1-((R)-3-{(S)-1-((1S,2R,3S)-1-Cyclohexylmethyl-2,3-dihydroxy-5-pyridin-2-yl-pentylcarbamoyl)-2-[1-(2,4-dinitro-phenyl)-1H-imidazol-4-yl]-ethylcarbamoyl}-4-naphthalen-1-yl-butyryl)-piperidin-4-yl]-carbamic acid tert-butyl ester

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Technology Process of [1-((R)-3-{(S)-1-((1S,2R,3S)-1-Cyclohexylmethyl-2,3-dihydroxy-5-pyridin-2-yl-pentylcarbamoyl)-2-[1-(2,4-dinitro-phenyl)-1H-imidazol-4-yl]-ethylcarbamoyl}-4-naphthalen-1-yl-butyryl)-piperidin-4-yl]-carbamic acid tert-butyl ester

There total 11 articles about [1-((R)-3-{(S)-1-((1S,2R,3S)-1-Cyclohexylmethyl-2,3-dihydroxy-5-pyridin-2-yl-pentylcarbamoyl)-2-[1-(2,4-dinitro-phenyl)-1H-imidazol-4-yl]-ethylcarbamoyl}-4-naphthalen-1-yl-butyryl)-piperidin-4-yl]-carbamic acid tert-butyl 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: 64.1%

: 135632-43-8
(2R)-3-<<1-<4-<(tert-butyloxycarbonyl)amino>piperidinyl>>carbonyl>-2-<(1-naphthyl)methyl>propionic acid

: 150577-71-2
N-im-(2,4-dinitrophenyl)-L-histidyl>-(2S,3R,4S)-1-cyclohexyl-3,4-dihydroxy-6-(2-pyridyl)hexan-2-amine

: 135650-90-7
[1-((R)-3-{(S)-1-((1S,2R,3S)-1-Cyclohexylmethyl-2,3-dihydroxy-5-pyridin-2-yl-pentylcarbamoyl)-2-[1-(2,4-dinitro-phenyl)-1H-imidazol-4-yl]-ethylcarbamoyl}-4-naphthalen-1-yl-butyryl)-piperidin-4-yl]-carbamic acid tert-butyl ester

Guidance literature:: With N-ethylmorpholine;; benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; In acetonitrile; for 2h; Ambient temperature;
DOI:10.1021/jm00071a009

Reference yield:

: 99124-56-8
3-(1-naphthalenyl)propionyl chloride

: 135650-90-7
[1-((R)-3-{(S)-1-((1S,2R,3S)-1-Cyclohexylmethyl-2,3-dihydroxy-5-pyridin-2-yl-pentylcarbamoyl)-2-[1-(2,4-dinitro-phenyl)-1H-imidazol-4-yl]-ethylcarbamoyl}-4-naphthalen-1-yl-butyryl)-piperidin-4-yl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) n-butyllithium / 1.) THF, hexane, -78 deg C, 2 h, 2.) THF, hexane, RT, 2 h

2: 1.) n-butyllithium, diisopropylamine / 1.) THF, n-hexane, -78 deg C, 1 h, 2.) THF, n-hexane, -78 deg C, 4 h

3: 91.4 percent / H₂ / 10percent Pd/C / ethanol

4: 61.3 percent / HOBt*H₂O, N-ethylmorpholine, HBTU / dimethylformamide / 2 h / Ambient temperature

5: 64.5 percent / LiOH*H₂O / tetrahydrofuran; H₂O / 3 h / 0 °C

6: 64.1 percent / HOBt*H₂O, N-ethylmorpholine, HBTU / acetonitrile / 2 h / Ambient temperature

With N-ethylmorpholine;; lithium hydroxide; n-butyllithium; hydrogen; benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; diisopropylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm00071a009

Reference yield:

: 119377-27-4
(4S)-3-<3-(1-naphthyl)propionyl>-4-benzyloxazolidin-2-one

: 135650-90-7
[1-((R)-3-{(S)-1-((1S,2R,3S)-1-Cyclohexylmethyl-2,3-dihydroxy-5-pyridin-2-yl-pentylcarbamoyl)-2-[1-(2,4-dinitro-phenyl)-1H-imidazol-4-yl]-ethylcarbamoyl}-4-naphthalen-1-yl-butyryl)-piperidin-4-yl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) n-butyllithium, diisopropylamine / 1.) THF, n-hexane, -78 deg C, 1 h, 2.) THF, n-hexane, -78 deg C, 4 h

2: 91.4 percent / H₂ / 10percent Pd/C / ethanol

3: 61.3 percent / HOBt*H₂O, N-ethylmorpholine, HBTU / dimethylformamide / 2 h / Ambient temperature

4: 64.5 percent / LiOH*H₂O / tetrahydrofuran; H₂O / 3 h / 0 °C

5: 64.1 percent / HOBt*H₂O, N-ethylmorpholine, HBTU / acetonitrile / 2 h / Ambient temperature

With N-ethylmorpholine;; lithium hydroxide; n-butyllithium; hydrogen; benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; diisopropylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm00071a009