{2-[2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-6-phenethyl-1,2,3,4-tetrahydro-naphthalen-2-yl}-carbamic acid tert-butyl ester

Base Information

Chemical Name:{2-[2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-6-phenethyl-1,2,3,4-tetrahydro-naphthalen-2-yl}-carbamic acid tert-butyl ester
CAS No.:936633-52-2
Molecular Formula:C₄₁H₄₈N₄O₅
Molecular Weight:676.856
Hs Code.:

{2-[2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-6-phenethyl-1,2,3,4-tetrahydro-naphthalen-2-yl}-carbamic acid <i>tert</i>-butyl ester

Synonyms:{2-[2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-6-phenethyl-1,2,3,4-tetrahydro-naphthalen-2-yl}-carbamic acid tert-butyl ester

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Chemical Property of {2-[2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-6-phenethyl-1,2,3,4-tetrahydro-naphthalen-2-yl}-carbamic acid tert-butyl ester

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Technology Process of {2-[2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-6-phenethyl-1,2,3,4-tetrahydro-naphthalen-2-yl}-carbamic acid tert-butyl ester

There total 5 articles about {2-[2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-6-phenethyl-1,2,3,4-tetrahydro-naphthalen-2-yl}-carbamic acid tert-butyl 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:

: 6-bromo-2-tert-butoxycarbonylamino-1,2,3,4-tetrahydro-naphthalene-2-carboxylic acid methyl ester

: 936633-52-2
{2-[2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-6-phenethyl-1,2,3,4-tetrahydro-naphthalen-2-yl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 78 percent / cesium carbonate; molecular sieves 4 Angstroem / P(t-Bu)3; Pd₂(dba)3 / dioxane / 18 h / Heating

2: 100 percent / hydrogen / Pd/C / ethyl acetate / 20 °C

3: 85 percent / lithium hydroxide monohydrate / tetrahydrofuran; methanol; H₂O / 20 °C

4: N-hydroxybenzotriazole hydrate; N,N'-diisopropylcarbodiimide / dimethylformamide / 15 h / 20 °C

With lithium hydroxide; 4 A molecular sieve; hydrogen; benzotriazol-1-ol; caesium carbonate; diisopropyl-carbodiimide; palladium on activated charcoal; tris(dibenzylideneacetone)dipalladium ⁽⁰⁾; tri-tert-butyl phosphine; In tetrahydrofuran; 1,4-dioxane; methanol; water; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm0614073

Reference yield:

: 100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6
styrene

: 936633-52-2
{2-[2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-6-phenethyl-1,2,3,4-tetrahydro-naphthalen-2-yl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 78 percent / cesium carbonate; molecular sieves 4 Angstroem / P(t-Bu)3; Pd₂(dba)3 / dioxane / 18 h / Heating

2: 100 percent / hydrogen / Pd/C / ethyl acetate / 20 °C

3: 85 percent / lithium hydroxide monohydrate / tetrahydrofuran; methanol; H₂O / 20 °C

4: N-hydroxybenzotriazole hydrate; N,N'-diisopropylcarbodiimide / dimethylformamide / 15 h / 20 °C

With lithium hydroxide; 4 A molecular sieve; hydrogen; benzotriazol-1-ol; caesium carbonate; diisopropyl-carbodiimide; palladium on activated charcoal; tris(dibenzylideneacetone)dipalladium ⁽⁰⁾; tri-tert-butyl phosphine; In tetrahydrofuran; 1,4-dioxane; methanol; water; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm0614073

Reference yield:

: 936633-45-3
2-tert-butoxycarbonylamino-6-styryl-1,2,3,4-tetrahydro-naphthalene-2-carboxylic acid methyl ester

: 936633-52-2
{2-[2-carbamoyl-1-(3-naphthalen-1-yl-propylcarbamoyl)-ethylcarbamoyl]-6-phenethyl-1,2,3,4-tetrahydro-naphthalen-2-yl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / hydrogen / Pd/C / ethyl acetate / 20 °C

2: 85 percent / lithium hydroxide monohydrate / tetrahydrofuran; methanol; H₂O / 20 °C

3: N-hydroxybenzotriazole hydrate; N,N'-diisopropylcarbodiimide / dimethylformamide / 15 h / 20 °C

With lithium hydroxide; hydrogen; benzotriazol-1-ol; diisopropyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; methanol; water; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm0614073