(5R,6S,7S,8S)-8-acetoxy-6,7-bis(benzyloxy)-5-benzyloxymethyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine

Base Information

Chemical Name:(5R,6S,7S,8S)-8-acetoxy-6,7-bis(benzyloxy)-5-benzyloxymethyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine
CAS No.:162491-52-3
Molecular Formula:C₃₁H₃₂N₂O₅
Molecular Weight:512.605
Hs Code.:

Synonyms:(5R,6S,7S,8S)-8-acetoxy-6,7-bis(benzyloxy)-5-benzyloxymethyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine

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Chemical Property of (5R,6S,7S,8S)-8-acetoxy-6,7-bis(benzyloxy)-5-benzyloxymethyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine

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Technology Process of (5R,6S,7S,8S)-8-acetoxy-6,7-bis(benzyloxy)-5-benzyloxymethyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine

There total 9 articles about (5R,6S,7S,8S)-8-acetoxy-6,7-bis(benzyloxy)-5-benzyloxymethyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine 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: 98.0%

: 108-24-7
acetic anhydride

: 162438-96-2
2-[(1S,2R,3S,4S)-2,3,5-tris(benzyloxy)-4-benzylsulfonyloxy-1-hydroxypent-1-yl]-N-triphenylmethylimidazole

: 162491-52-3
(5R,6S,7S,8S)-8-acetoxy-6,7-bis(benzyloxy)-5-benzyloxymethyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine

Guidance literature:: With pyridine; at 60 ℃; for 1.5h;
DOI:10.1246/bcsj.70.427

Reference yield:

: 16838-89-4,17073-88-0,60933-68-8,60933-69-9,73068-66-3,89361-52-4,89615-42-9,89615-45-2,96192-07-3
2,3,5-tri-O-benzyl-α-L-ribofuranose

: 162491-52-3
(5R,6S,7S,8S)-8-acetoxy-6,7-bis(benzyloxy)-5-benzyloxymethyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-BuLi / tetrahydrofuran; hexane / 0.17 h / -5 °C

1.2: 40 percent / tetrahydrofuran; hexane / 0.5 h / 0 - 20 °C

2.1: 86 percent / pyridine / 1 h / 0 °C

3.1: 98 percent / pyridine / 1.5 h / 60 °C

With pyridine; n-butyllithium; In tetrahydrofuran; hexane; 1.1: Metallation / 1.2: Addition / 2.1: sulfonylation / 3.1: Cyclization;
DOI:10.1246/bcsj.70.427

Reference yield:

: 100-39-0
benzyl bromide

: 162491-52-3
(5R,6S,7S,8S)-8-acetoxy-6,7-bis(benzyloxy)-5-benzyloxymethyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine

Guidance literature:: Multi-step reaction with 5 steps

1: NaH / dimethylformamide / 0 °C

2: 0.05N HCl / dioxane / 105 °C

3: 1.) nBuLi / tetrahydrofuran / 0.5 h / 0 °C

4: 86 percent / pyridine / 1 h / -10 °C

5: 90 percent / pyridine / 1.5 h / 65 °C

With pyridine; hydrogenchloride; n-butyllithium; sodium hydride; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.1016/0040-4039(94)02460-S