(2S,3R,4S)-N-(N^im-trityl-L-histidyl)-1-cyclohexyl-3,4-dihydroxy-6-(2-pyridyl)hexan-2-amine

Base Information

• Chemical Name: (2S,3R,4S)-N-(N^im-trityl-L-histidyl)-1-cyclohexyl-3,4-dihydroxy-6-(2-pyridyl)hexan-2-amine
• CAS No.: 150544-99-3
• Molecular Formula: C₄₂H₄₉N₅O₃
• Molecular Weight: 671.883

Synonyms:(2S,3R,4S)-N-(N^im-trityl-L-histidyl)-1-cyclohexyl-3,4-dihydroxy-6-(2-pyridyl)hexan-2-amine

Chemical Property of (2S,3R,4S)-N-(N^im-trityl-L-histidyl)-1-cyclohexyl-3,4-dihydroxy-6-(2-pyridyl)hexan-2-amine

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Technology Process of (2S,3R,4S)-N-(N^im-trityl-L-histidyl)-1-cyclohexyl-3,4-dihydroxy-6-(2-pyridyl)hexan-2-amine

There total 3 articles about (2S,3R,4S)-N-(N^im-trityl-L-histidyl)-1-cyclohexyl-3,4-dihydroxy-6-(2-pyridyl)hexan-2-amine 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: 100.0%

(S)-N-{(S)-2-Cyclohexyl-1-[(4R,5S)-2,2-dimethyl-5-(2-pyridin-2-yl-ethyl)-[1,3]dioxolan-4-yl]-ethyl}-2-(trityl-amino)-3-(1-trityl-1H-imidazol-4-yl)-propionamide → (2S,3R,4S)-N-(Nim-trityl-L-histidyl)-1-cyclohexyl-3,4-dihydroxy-6-(2-pyridyl)hexan-2-amine (150544-99-3)

Guidance literature:

With hydrogenchloride; acetic acid; for 0.166667h;

DOI:10.1021/jm00071a009

Reference yield:

(2R,3R,4S)-2-amino-1-cyclohexyl-3,4-dihydroxy-6-(2-pyridyl)-3,4-acetonide → (2S,3R,4S)-N-(Nim-trityl-L-histidyl)-1-cyclohexyl-3,4-dihydroxy-6-(2-pyridyl)hexan-2-amine (150544-99-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 70.5 percent / HOBt*H₂O, N-ethylmorpholine, HBTU / acetonitrile / 2 h / Ambient temperature

2: 100 percent / glacial AcOH, aq. HCl / 0.17 h

With N-ethylmorpholine;; hydrogenchloride; benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; acetic acid; In acetonitrile;

DOI:10.1021/jm00071a009

Reference yield:

Nα,Nim-ditritylhistidine (74853-62-6) → (2S,3R,4S)-N-(Nim-trityl-L-histidyl)-1-cyclohexyl-3,4-dihydroxy-6-(2-pyridyl)hexan-2-amine (150544-99-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 70.5 percent / HOBt*H₂O, N-ethylmorpholine, HBTU / acetonitrile / 2 h / Ambient temperature

2: 100 percent / glacial AcOH, aq. HCl / 0.17 h

With N-ethylmorpholine;; hydrogenchloride; benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; acetic acid; In acetonitrile;

DOI:10.1021/jm00071a009

upstream raw materials:

N^α,N^im-ditritylhistidine

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