4-{5-(3-tert-butoxycarbonyl-propoxy)-2-[2,4-dimethoxy-5-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-5-methyl-phenylcarbamoyl)-phenylcarbamoyl]-4-nitro-phenoxy}-butyric acid tert-butyl ester

Base Information

Chemical Name:4-{5-(3-tert-butoxycarbonyl-propoxy)-2-[2,4-dimethoxy-5-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-5-methyl-phenylcarbamoyl)-phenylcarbamoyl]-4-nitro-phenoxy}-butyric acid tert-butyl ester
CAS No.:874210-74-9
Molecular Formula:C₄₆H₆₃N₃O₁₆
Molecular Weight:914.017
Hs Code.:

4-{5-(3-<i>tert</i>-butoxycarbonyl-propoxy)-2-[2,4-dimethoxy-5-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-5-methyl-phenylcarbamoyl)-phenylcarbamoyl]-4-nitro-phenoxy}-butyric acid <i>tert</i>-butyl ester

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Chemical Property of 4-{5-(3-tert-butoxycarbonyl-propoxy)-2-[2,4-dimethoxy-5-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-5-methyl-phenylcarbamoyl)-phenylcarbamoyl]-4-nitro-phenoxy}-butyric acid tert-butyl ester

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Technology Process of 4-{5-(3-tert-butoxycarbonyl-propoxy)-2-[2,4-dimethoxy-5-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-5-methyl-phenylcarbamoyl)-phenylcarbamoyl]-4-nitro-phenoxy}-butyric acid tert-butyl ester

There total 13 articles about 4-{5-(3-tert-butoxycarbonyl-propoxy)-2-[2,4-dimethoxy-5-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-5-methyl-phenylcarbamoyl)-phenylcarbamoyl]-4-nitro-phenoxy}-butyric 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:

: 271261-74-6
2,4-dimethoxy-5-nitro-benzoyl chloride

: 874210-74-9
4-{5-(3-tert-butoxycarbonyl-propoxy)-2-[2,4-dimethoxy-5-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-5-methyl-phenylcarbamoyl)-phenylcarbamoyl]-4-nitro-phenoxy}-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: 6.1 g / triethylamine / CH₂Cl₂ / 20 °C

2.1: H₂ / Pd/C / ethanol; CHCl₃ / 5 h / 40 °C / 0.03 Torr

3.1: EDC; 1-hydroxybenzotriazole / CH₂Cl₂ / 0.83 h / 20 °C

3.2: 537 mg / triethylamine / CH₂Cl₂ / 20 °C

With hydrogen; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; palladium on activated charcoal; In ethanol; dichloromethane; chloroform;
DOI:10.1021/jo050798a

Reference yield:

: 827325-28-0
2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-5-methyl-phenylamine

: 874210-74-9
4-{5-(3-tert-butoxycarbonyl-propoxy)-2-[2,4-dimethoxy-5-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-5-methyl-phenylcarbamoyl)-phenylcarbamoyl]-4-nitro-phenoxy}-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: 6.1 g / triethylamine / CH₂Cl₂ / 20 °C

2.1: H₂ / Pd/C / ethanol; CHCl₃ / 5 h / 40 °C / 0.03 Torr

3.1: EDC; 1-hydroxybenzotriazole / CH₂Cl₂ / 0.83 h / 20 °C

3.2: 537 mg / triethylamine / CH₂Cl₂ / 20 °C

With hydrogen; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; palladium on activated charcoal; In ethanol; dichloromethane; chloroform;
DOI:10.1021/jo050798a

Reference yield:

: 874210-48-7
1-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}-4-methyl-2-nitrobenzene

: 874210-74-9
4-{5-(3-tert-butoxycarbonyl-propoxy)-2-[2,4-dimethoxy-5-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-5-methyl-phenylcarbamoyl)-phenylcarbamoyl]-4-nitro-phenoxy}-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: H₂ / Pd/C / ethanol / 2 h / 0.01 Torr

2.1: 6.1 g / triethylamine / CH₂Cl₂ / 20 °C

3.1: H₂ / Pd/C / ethanol; CHCl₃ / 5 h / 40 °C / 0.03 Torr

4.1: EDC; 1-hydroxybenzotriazole / CH₂Cl₂ / 0.83 h / 20 °C

4.2: 537 mg / triethylamine / CH₂Cl₂ / 20 °C

With hydrogen; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; palladium on activated charcoal; In ethanol; dichloromethane; chloroform;
DOI:10.1021/jo050798a