1,3,4-tri-O-benzyl-1-(1-triphenylmethyl-1H-imidazol-4-yl)-5-O-triphenylmethyl-L-ido-pentitol

Base Information

Chemical Name:1,3,4-tri-O-benzyl-1-(1-triphenylmethyl-1H-imidazol-4-yl)-5-O-triphenylmethyl-L-ido-pentitol
CAS No.:613234-41-6
Molecular Formula:C₆₇H₆₀N₂O₅
Molecular Weight:973.224
Hs Code.:

Synonyms:1,3,4-tri-O-benzyl-1-(1-triphenylmethyl-1H-imidazol-4-yl)-5-O-triphenylmethyl-L-ido-pentitol

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Chemical Property of 1,3,4-tri-O-benzyl-1-(1-triphenylmethyl-1H-imidazol-4-yl)-5-O-triphenylmethyl-L-ido-pentitol

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Technology Process of 1,3,4-tri-O-benzyl-1-(1-triphenylmethyl-1H-imidazol-4-yl)-5-O-triphenylmethyl-L-ido-pentitol

There total 6 articles about 1,3,4-tri-O-benzyl-1-(1-triphenylmethyl-1H-imidazol-4-yl)-5-O-triphenylmethyl-L-ido-pentitol 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: 37.0%

: 100-39-0
benzyl bromide

: 613234-39-2
1,3-di-O-benzyl-1-(1-triphenylmethyl-1H-imidazol-4-yl)-5-O-triphenylmethyl-L-ido-pentitol

: 613234-41-6
1,3,4-tri-O-benzyl-1-(1-triphenylmethyl-1H-imidazol-4-yl)-5-O-triphenylmethyl-L-ido-pentitol

: 1,3,4-tri-O-benzyl-1-(1-triphenylmethyl-1H-imidazol-4-yl)-5-O-triphenylmethyl-L-ido-pentitol

Guidance literature:: With tetra-(n-butyl)ammonium iodide; sodium hydride; In tetrahydrofuran; at 0 - 20 ℃;
DOI:10.1016/S0040-4020(03)01055-X

Reference yield:

: 23558-05-6
3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose

: 613234-41-6
1,3,4-tri-O-benzyl-1-(1-triphenylmethyl-1H-imidazol-4-yl)-5-O-triphenylmethyl-L-ido-pentitol

Guidance literature:: Multi-step reaction with 6 steps

1.1: n-BuLi / hexane; tetrahydrofuran / 0.25 h / -70 °C

1.2: 31 percent / hexane; tetrahydrofuran / 2.75 h / -70 - 20 °C

2.1: NaH / dimethylformamide; various solvent(s) / 0 - 20 °C

3.1: 2.53 g / hydrochloric acid / H₂O; tetrahydrofuran / 1.5 h / Heating

4.1: 88 percent / NaBH₄ / methanol / 0 - 20 °C

5.1: 56 percent / 4-(dimethylamino)pyridine; pyridine / 48 h / 80 - 90 °C

6.1: 37 percent / NaH; n-BuN₄I / tetrahydrofuran; various solvent(s) / 0 - 20 °C

With pyridine; hydrogenchloride; dmap; sodium tetrahydroborate; n-butyllithium; tetra-(n-butyl)ammonium iodide; sodium hydride; In tetrahydrofuran; methanol; hexane; water; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(03)01055-X

Reference yield:

: (5S)-3,5-di-O-benzyl-5-[1H-imidazol-4⁽⁵⁾-yl]-D-xylofuranose

: 613234-41-6
1,3,4-tri-O-benzyl-1-(1-triphenylmethyl-1H-imidazol-4-yl)-5-O-triphenylmethyl-L-ido-pentitol

Guidance literature:: Multi-step reaction with 3 steps

1: 88 percent / NaBH₄ / methanol / 0 - 20 °C

2: 56 percent / 4-(dimethylamino)pyridine; pyridine / 48 h / 80 - 90 °C

3: 37 percent / NaH; n-BuN₄I / tetrahydrofuran; various solvent(s) / 0 - 20 °C

With pyridine; dmap; sodium tetrahydroborate; tetra-(n-butyl)ammonium iodide; sodium hydride; In tetrahydrofuran; methanol;
DOI:10.1016/S0040-4020(03)01055-X