(S)-N-(benzo[d][1,3]dioxol-5-yl)-2-(2-(1-ethyl-2,4,7-trimethyl-1H-indol-3-yl)acetamido)-N-methyl-3-phenylpropanamide

Base Information

Chemical Name:(S)-N-(benzo[d][1,3]dioxol-5-yl)-2-(2-(1-ethyl-2,4,7-trimethyl-1H-indol-3-yl)acetamido)-N-methyl-3-phenylpropanamide
CAS No.:1375275-51-6
Molecular Formula:C₃₂H₃₅N₃O₄
Molecular Weight:525.648
Hs Code.:

Synonyms:(S)-N-(benzo[d][1,3]dioxol-5-yl)-2-(2-(1-ethyl-2,4,7-trimethyl-1H-indol-3-yl)acetamido)-N-methyl-3-phenylpropanamide

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Chemical Property of (S)-N-(benzo[d][1,3]dioxol-5-yl)-2-(2-(1-ethyl-2,4,7-trimethyl-1H-indol-3-yl)acetamido)-N-methyl-3-phenylpropanamide

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Technology Process of (S)-N-(benzo[d][1,3]dioxol-5-yl)-2-(2-(1-ethyl-2,4,7-trimethyl-1H-indol-3-yl)acetamido)-N-methyl-3-phenylpropanamide

There total 8 articles about (S)-N-(benzo[d][1,3]dioxol-5-yl)-2-(2-(1-ethyl-2,4,7-trimethyl-1H-indol-3-yl)acetamido)-N-methyl-3-phenylpropanamide 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: 50.0%

: 1375278-22-0
2-(1-ethyl-2,4,7-trimethyl-1H-indol-3-yl)acetic acid

: 1375278-24-2
(S)-2-amino-N-(benzo[d][1,3]dioxol-5-yl)-N-methyl-3-phenylpropanamide hydrochloride

: 1375275-51-6
(S)-N-(benzo[d][1,3]dioxol-5-yl)-2-(2-(1-ethyl-2,4,7-trimethyl-1H-indol-3-yl)acetamido)-N-methyl-3-phenylpropanamide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap; In dichloromethane; at 20 ℃;

Reference yield:

: 95-78-3
2,5-Dimethylaniline

: 1375275-51-6
(S)-N-(benzo[d][1,3]dioxol-5-yl)-2-(2-(1-ethyl-2,4,7-trimethyl-1H-indol-3-yl)acetamido)-N-methyl-3-phenylpropanamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogenchloride; sodium nitrite / water / 1 h / 0 - 5 °C

1.2: 0 - 20 °C

1.3: 0 °C

2.1: sodium hydrogencarbonate / dichloromethane; water / 3 h / 20 °C

2.2: 140 °C

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.67 h / 20 °C

3.2: 4 h / 0 - 50 °C

3.3: pH 5

4.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dmap / dichloromethane / 20 °C

With hydrogenchloride; sodium hydride; sodium hydrogencarbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium nitrite; dmap; In dichloromethane; water; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 613-85-4
(2,5-dimethylphenyl)hydrazine

: 1375275-51-6
(S)-N-(benzo[d][1,3]dioxol-5-yl)-2-(2-(1-ethyl-2,4,7-trimethyl-1H-indol-3-yl)acetamido)-N-methyl-3-phenylpropanamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydrogencarbonate / dichloromethane; water / 3 h / 20 °C

1.2: 140 °C

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.67 h / 20 °C

2.2: 4 h / 0 - 50 °C

2.3: pH 5

3.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dmap / dichloromethane / 20 °C

With sodium hydride; sodium hydrogencarbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap; In dichloromethane; water; N,N-dimethyl-formamide; mineral oil;