({4-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-benzoimidazol-2-yl]furazan-3-ylcarbamoyl}methyl)carbamic acid benzyl ester

Base Information

Chemical Name:({4-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-benzoimidazol-2-yl]furazan-3-ylcarbamoyl}methyl)carbamic acid benzyl ester
CAS No.:1263384-56-0
Molecular Formula:C₂₅H₃₀N₆O₅Si
Molecular Weight:522.636
Hs Code.:

Synonyms:({4-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-benzoimidazol-2-yl]furazan-3-ylcarbamoyl}methyl)carbamic acid benzyl ester

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Chemical Property of ({4-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-benzoimidazol-2-yl]furazan-3-ylcarbamoyl}methyl)carbamic acid benzyl ester

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Technology Process of ({4-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-benzoimidazol-2-yl]furazan-3-ylcarbamoyl}methyl)carbamic acid benzyl ester

There total 5 articles about ({4-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-benzoimidazol-2-yl]furazan-3-ylcarbamoyl}methyl)carbamic acid benzyl 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:

: 332026-86-5
3-amino-4-(1H-benzo[d]imidazol-2-yl)-1,2,5-oxadiazole

: 1263384-56-0
({4-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-benzoimidazol-2-yl]furazan-3-ylcarbamoyl}methyl)carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydride / tetrahydrofuran / 0.17 h / 0 - 5 °C

1.2: 0.5 h / 0 - 5 °C

2.1: sodium hydride / tetrahydrofuran / 0 - 70 °C / sealed tube

With sodium hydride; In tetrahydrofuran;

Reference yield:

: 15050-24-5
N-(benzyloxycarbonyl)glycyl chloride

: 1263384-55-9
4-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-benzoimidazol-2-yl]furazan-3-ylamine

: 1263384-56-0
({4-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-benzoimidazol-2-yl]furazan-3-ylcarbamoyl}methyl)carbamic acid benzyl ester

Guidance literature:: With sodium hydride; In tetrahydrofuran; at 0 - 70 ℃; sealed tube;

Reference yield:

: 63823-75-6
α-hydroxyimino-(1H-benzimidazol-2-yl) acetonitrile

: 1263384-56-0
({4-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-benzoimidazol-2-yl]furazan-3-ylcarbamoyl}methyl)carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydroxylamine hydrochloride; potassium hydroxide / diethylene glycol dimethyl ether / 170 °C / Cooling with ice

2.1: sodium hydride / tetrahydrofuran / 0.17 h / 0 - 5 °C

2.2: 0.5 h / 0 - 5 °C

3.1: sodium hydride / tetrahydrofuran / 0 - 70 °C / sealed tube

With hydroxylamine hydrochloride; sodium hydride; potassium hydroxide; In tetrahydrofuran; diethylene glycol dimethyl ether;