N-cyclohexylmethyl-2-(6-methoxy-1H-indol-3-yl)-2-oxo-N-(1H-tetrazol-5-ylmethyl)acetamide

Base Information

Chemical Name:N-cyclohexylmethyl-2-(6-methoxy-1H-indol-3-yl)-2-oxo-N-(1H-tetrazol-5-ylmethyl)acetamide
CAS No.:1192477-00-1
Molecular Formula:C₂₀H₂₄N₆O₃
Molecular Weight:396.449
Hs Code.:

Synonyms:N-cyclohexylmethyl-2-(6-methoxy-1H-indol-3-yl)-2-oxo-N-(1H-tetrazol-5-ylmethyl)acetamide

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Chemical Property of N-cyclohexylmethyl-2-(6-methoxy-1H-indol-3-yl)-2-oxo-N-(1H-tetrazol-5-ylmethyl)acetamide

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Technology Process of N-cyclohexylmethyl-2-(6-methoxy-1H-indol-3-yl)-2-oxo-N-(1H-tetrazol-5-ylmethyl)acetamide

There total 8 articles about N-cyclohexylmethyl-2-(6-methoxy-1H-indol-3-yl)-2-oxo-N-(1H-tetrazol-5-ylmethyl)acetamide 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: 57.0%

: 1192477-80-7
C₂₀H₂₃N₃O₃

: 1192477-00-1
N-cyclohexylmethyl-2-(6-methoxy-1H-indol-3-yl)-2-oxo-N-(1H-tetrazol-5-ylmethyl)acetamide

Guidance literature:: With sodium azide; ammonium chloride; In N,N-dimethyl-formamide; at 120 ℃;

Reference yield:

: 2043-61-0
cyclohexanecarbaldehyde

: 1192477-00-1
N-cyclohexylmethyl-2-(6-methoxy-1H-indol-3-yl)-2-oxo-N-(1H-tetrazol-5-ylmethyl)acetamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: triethylamine / methanol / 1 h / 0 °C

1.2: 18 h / 20 °C

2.1: sodium hydrogencarbonate / water; toluene / 1 h / 20 °C

3.1: hydrogenchloride / 1,4-dioxane / 18 h / 20 °C

4.1: 2-(1H-9-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluroniumhexafluorophosphate; ammonia; N-ethyl-N,N-diisopropylamine / dichloromethane; N,N-dimethyl-formamide / 18 h / 20 °C

5.1: pyridine; trifluoroacetic anhydride / tetrahydrofuran / 20 °C

6.1: sodium azide; ammonium chloride / N,N-dimethyl-formamide / 120 °C

With pyridine; hydrogenchloride; sodium azide; 2-(1H-9-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluroniumhexafluorophosphate; ammonia; sodium hydrogencarbonate; ammonium chloride; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic anhydride; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; water; N,N-dimethyl-formamide; toluene;

Reference yield:

: 1192476-88-2
{cyclohexylmethyl-[2-(6-methoxy-1H-indol-3-yl)-2-oxo-acetyl]amino}acetic acid

: 1192477-00-1
N-cyclohexylmethyl-2-(6-methoxy-1H-indol-3-yl)-2-oxo-N-(1H-tetrazol-5-ylmethyl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: 2-(1H-9-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluroniumhexafluorophosphate; ammonia; N-ethyl-N,N-diisopropylamine / dichloromethane; N,N-dimethyl-formamide / 18 h / 20 °C

2: pyridine; trifluoroacetic anhydride / tetrahydrofuran / 20 °C

3: sodium azide; ammonium chloride / N,N-dimethyl-formamide / 120 °C

With pyridine; sodium azide; 2-(1H-9-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluroniumhexafluorophosphate; ammonia; ammonium chloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic anhydride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;