-carbamic acid <1-(1H-indol-3-ylmethyl)-1-methyl-2-oxo-2-<<2-<<1-oxo-3-(1H-tetrazol-5-yl)propyl>amino>-2-phenylethyl>amino>ethyl>tricyclo<3.3.1.1^3,7>dec-2-yl ester

Base Information

• Chemical Name: -carbamic acid <1-(1H-indol-3-ylmethyl)-1-methyl-2-oxo-2-<<2-<<1-oxo-3-(1H-tetrazol-5-yl)propyl>amino>-2-phenylethyl>amino>ethyl>tricyclo<3.3.1.1^3,7>dec-2-yl ester
• CAS No.: 134557-55-4
• Molecular Formula: C₃₅H₄₂N₈O₄
• Molecular Weight: 638.77

Synonyms:

Chemical Property of -carbamic acid <1-(1H-indol-3-ylmethyl)-1-methyl-2-oxo-2-<<2-<<1-oxo-3-(1H-tetrazol-5-yl)propyl>amino>-2-phenylethyl>amino>ethyl>tricyclo<3.3.1.1^3,7>dec-2-yl ester

Chemical Property:

Purity/Quality:

Safty Information:

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MSDS Files:

Useful:

Technology Process of -carbamic acid <1-(1H-indol-3-ylmethyl)-1-methyl-2-oxo-2-<<2-<<1-oxo-3-(1H-tetrazol-5-yl)propyl>amino>-2-phenylethyl>amino>ethyl>tricyclo<3.3.1.1^3,7>dec-2-yl ester

There total 1 articles about -carbamic acid <1-(1H-indol-3-ylmethyl)-1-methyl-2-oxo-2-<<2-<<1-oxo-3-(1H-tetrazol-5-yl)propyl>amino>-2-phenylethyl>amino>ethyl>tricyclo<3.3.1.1^3,7>dec-2-yl 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:

benzyl bromide (100-39-0) + tricyclo<3.3.1.13,7>dec-2-yl *,R*)>-<2-<(2-amino-2-phenylethyl)amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>carbamate (130406-64-3) + 1H-tetrazole-5-propanoic acid methyl ester (134558-05-7) → -carbamic acid <1-(1H-indol-3-ylmethyl)-1-methyl-2-oxo-2-<<2-<<1-oxo-3-(1H-tetrazol-5-yl)propyl>amino>-2-phenylethyl>amino>ethyl>tricyclo<3.3.1.13,7>dec-2-yl ester (134557-55-4)

Guidance literature:

With 1-hydroxybenzotriazol-hydrate; dicyclohexyl-carbodiimide; Yield given. Multistep reaction;

DOI:10.1016/0223-5234(93)90078-S

upstream raw materials:

benzyl bromide

tricyclo<3.3.1.1^3,7>dec-2-yl *,R^*)>-<2-<(2-amino-2-phenylethyl)amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>carbamate

1H-tetrazole-5-propanoic acid methyl ester

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