(3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-5-[3-(2-pyridin-2-yl-acetyl)-benzyl]-7-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazol-5-ylmethyl]-hexahydro-1,3-dioxa-5,7-diaza-azulen-6-one

Base Information

Chemical Name:(3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-5-[3-(2-pyridin-2-yl-acetyl)-benzyl]-7-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazol-5-ylmethyl]-hexahydro-1,3-dioxa-5,7-diaza-azulen-6-one
CAS No.:209804-82-0
Molecular Formula:C₅₀H₅₇N₅O₅Si
Molecular Weight:836.119
Hs Code.:

(3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-5-[3-(2-pyridin-2-yl-acetyl)-benzyl]-7-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazol-5-ylmethyl]-hexahydro-1,3-dioxa-5,7-diaza-azulen-6-one

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Chemical Property of (3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-5-[3-(2-pyridin-2-yl-acetyl)-benzyl]-7-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazol-5-ylmethyl]-hexahydro-1,3-dioxa-5,7-diaza-azulen-6-one

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Technology Process of (3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-5-[3-(2-pyridin-2-yl-acetyl)-benzyl]-7-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazol-5-ylmethyl]-hexahydro-1,3-dioxa-5,7-diaza-azulen-6-one

There total 5 articles about (3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-5-[3-(2-pyridin-2-yl-acetyl)-benzyl]-7-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazol-5-ylmethyl]-hexahydro-1,3-dioxa-5,7-diaza-azulen-6-one 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:

: 1129-28-8
3-methoxycarbonylbenzyl bromide

: 209804-82-0
(3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-5-[3-(2-pyridin-2-yl-acetyl)-benzyl]-7-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazol-5-ylmethyl]-hexahydro-1,3-dioxa-5,7-diaza-azulen-6-one

Guidance literature:: Multi-step reaction with 4 steps

1: NaH / dimethylformamide

2: 1N NaOH / dioxane / 24 h / Ambient temperature

3: CBr₄, Ph₃P, pyridine / CH₂Cl₂ / 1 h / Ambient temperature

4: 1.) PhLi / 1.) THF, RT, 1 h, 2.) THF, from -78 deg C to RT

With pyridine; sodium hydroxide; carbon tetrabromide; sodium hydride; phenyllithium; triphenylphosphine; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm980103g

Reference yield:

: (3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-5-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazol-5-ylmethyl]-hexahydro-1,3-dioxa-5,7-diaza-azulen-6-one

: 209804-82-0
(3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-5-[3-(2-pyridin-2-yl-acetyl)-benzyl]-7-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazol-5-ylmethyl]-hexahydro-1,3-dioxa-5,7-diaza-azulen-6-one

Guidance literature:: Multi-step reaction with 4 steps

1: NaH / dimethylformamide

2: 1N NaOH / dioxane / 24 h / Ambient temperature

3: CBr₄, Ph₃P, pyridine / CH₂Cl₂ / 1 h / Ambient temperature

4: 1.) PhLi / 1.) THF, RT, 1 h, 2.) THF, from -78 deg C to RT

With pyridine; sodium hydroxide; carbon tetrabromide; sodium hydride; phenyllithium; triphenylphosphine; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm980103g

Reference yield:

: (3aS,4R,8R,8aS)-4,8-Dibenzyl-6-methoxy-2,2-dimethyl-5-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazol-5-ylmethyl]-4,5,8,8a-tetrahydro-3aH-1,3-dioxa-5,7-diaza-azulene

: 209804-82-0
(3aS,4R,8R,8aS)-4,8-Dibenzyl-2,2-dimethyl-5-[3-(2-pyridin-2-yl-acetyl)-benzyl]-7-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-indazol-5-ylmethyl]-hexahydro-1,3-dioxa-5,7-diaza-azulen-6-one

Guidance literature:: Multi-step reaction with 4 steps

1: 1.2 g / KI / acetonitrile / 6 h / Heating

2: 1N NaOH / dioxane / 24 h / Ambient temperature

3: CBr₄, Ph₃P, pyridine / CH₂Cl₂ / 1 h / Ambient temperature

4: 1.) PhLi / 1.) THF, RT, 1 h, 2.) THF, from -78 deg C to RT

With pyridine; sodium hydroxide; carbon tetrabromide; phenyllithium; triphenylphosphine; potassium iodide; In 1,4-dioxane; dichloromethane; acetonitrile;
DOI:10.1021/jm980103g