N-[1-(1-tert-butylcarbamoyl-1-methyl-ethylcarbamoyl)-1-methyl-ethyl]-2-methyl-2-(3-tritylsulfanyl-propionylamino)-propionamide

Base Information

Chemical Name:N-[1-(1-tert-butylcarbamoyl-1-methyl-ethylcarbamoyl)-1-methyl-ethyl]-2-methyl-2-(3-tritylsulfanyl-propionylamino)-propionamide
CAS No.:875577-25-6
Molecular Formula:C₃₈H₅₀N₄O₄S
Molecular Weight:658.905
Hs Code.:

<i>N</i>-[1-(1-<i>tert</i>-butylcarbamoyl-1-methyl-ethylcarbamoyl)-1-methyl-ethyl]-2-methyl-2-(3-tritylsulfanyl-propionylamino)-propionamide

Synonyms:N-[1-(1-tert-butylcarbamoyl-1-methyl-ethylcarbamoyl)-1-methyl-ethyl]-2-methyl-2-(3-tritylsulfanyl-propionylamino)-propionamide

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Chemical Property of N-[1-(1-tert-butylcarbamoyl-1-methyl-ethylcarbamoyl)-1-methyl-ethyl]-2-methyl-2-(3-tritylsulfanyl-propionylamino)-propionamide

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Technology Process of N-[1-(1-tert-butylcarbamoyl-1-methyl-ethylcarbamoyl)-1-methyl-ethyl]-2-methyl-2-(3-tritylsulfanyl-propionylamino)-propionamide

There total 6 articles about N-[1-(1-tert-butylcarbamoyl-1-methyl-ethylcarbamoyl)-1-methyl-ethyl]-2-methyl-2-(3-tritylsulfanyl-propionylamino)-propionamide 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: 64.0%

: H-(Aib)3-NHtBu

: 27144-18-9
3-(tritylthio) propanoic acid

: 875577-25-6
N-[1-(1-tert-butylcarbamoyl-1-methyl-ethylcarbamoyl)-1-methyl-ethyl]-2-methyl-2-(3-tritylsulfanyl-propionylamino)-propionamide

Guidance literature:: With 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 24h;
DOI:10.1021/ja0560581

Reference yield:

: H-Aib-NHtBu

: 875577-25-6
N-[1-(1-tert-butylcarbamoyl-1-methyl-ethylcarbamoyl)-1-methyl-ethyl]-2-methyl-2-(3-tritylsulfanyl-propionylamino)-propionamide

Guidance literature:: Multi-step reaction with 5 steps

1: 70 percent / 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; 1-hydroxy-7-aza-1,2,3-benzotriazole; N,N-diisopropylethylamine / CH₂Cl₂ / 12 h / 20 °C

2: methanol / catalytic hydrogenation

3: 67 percent / 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; 1-hydroxy-7-aza-1,2,3-benzotriazole; N,N-diisopropylethylamine / CH₂Cl₂ / 14 h / 20 °C

4: methanol / catalytic hydrogenation

5: 64 percent / 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; 1-hydroxy-7-aza-1,2,3-benzotriazole; N,N-diisopropylethylamine / CH₂Cl₂ / 24 h / 20 °C

With 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane;
DOI:10.1021/ja0560581

Reference yield:

: 2-(2-amino-2-methyl-propionylamino)-N-tert-butyl-2-methyl-propionamide

: 875577-25-6
N-[1-(1-tert-butylcarbamoyl-1-methyl-ethylcarbamoyl)-1-methyl-ethyl]-2-methyl-2-(3-tritylsulfanyl-propionylamino)-propionamide

Guidance literature:: Multi-step reaction with 3 steps

1: 67 percent / 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; 1-hydroxy-7-aza-1,2,3-benzotriazole; N,N-diisopropylethylamine / CH₂Cl₂ / 14 h / 20 °C

2: methanol / catalytic hydrogenation

3: 64 percent / 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; 1-hydroxy-7-aza-1,2,3-benzotriazole; N,N-diisopropylethylamine / CH₂Cl₂ / 24 h / 20 °C

With 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane;
DOI:10.1021/ja0560581