(S)-N-(benzo[d][1,3]dioxol-5-yl)-N-methyl-2-(2-(2-methyl-3-vinyl-1H-pyrrolo[2,3-b]pyridin-1-yl)acetamido)-3-phenylpropanamide

Base Information

Chemical Name:(S)-N-(benzo[d][1,3]dioxol-5-yl)-N-methyl-2-(2-(2-methyl-3-vinyl-1H-pyrrolo[2,3-b]pyridin-1-yl)acetamido)-3-phenylpropanamide
CAS No.:1375278-66-2
Molecular Formula:C₂₉H₂₈N₄O₄
Molecular Weight:496.566
Hs Code.:

Synonyms:(S)-N-(benzo[d][1,3]dioxol-5-yl)-N-methyl-2-(2-(2-methyl-3-vinyl-1H-pyrrolo[2,3-b]pyridin-1-yl)acetamido)-3-phenylpropanamide

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Chemical Property of (S)-N-(benzo[d][1,3]dioxol-5-yl)-N-methyl-2-(2-(2-methyl-3-vinyl-1H-pyrrolo[2,3-b]pyridin-1-yl)acetamido)-3-phenylpropanamide

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Technology Process of (S)-N-(benzo[d][1,3]dioxol-5-yl)-N-methyl-2-(2-(2-methyl-3-vinyl-1H-pyrrolo[2,3-b]pyridin-1-yl)acetamido)-3-phenylpropanamide

There total 5 articles about (S)-N-(benzo[d][1,3]dioxol-5-yl)-N-methyl-2-(2-(2-methyl-3-vinyl-1H-pyrrolo[2,3-b]pyridin-1-yl)acetamido)-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: 17.0%

: 1375278-65-1
2-(2-methyl-3-vinyl-1H-pyrrolo[2,3-b]pyridin-1-yl)acetic acid

: 1375278-62-8
(S)-2-amino-N-(benzo[d][1,3]dioxol-5-yl)-N-methyl-3-phenylpropanamide

: 1375278-66-2
(S)-N-(benzo[d][1,3]dioxol-5-yl)-N-methyl-2-(2-(2-methyl-3-vinyl-1H-pyrrolo[2,3-b]pyridin-1-yl)acetamido)-3-phenylpropanamide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; Inert atmosphere;

Reference yield:

: 23612-48-8
2-methyl-1H-pyrrolo[2,3-b]pyridine

: 1375278-66-2
(S)-N-(benzo[d][1,3]dioxol-5-yl)-N-methyl-2-(2-(2-methyl-3-vinyl-1H-pyrrolo[2,3-b]pyridin-1-yl)acetamido)-3-phenylpropanamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium hydroxide / N,N-dimethyl-formamide / 0.5 h / 0 - 20 °C

1.2: 0 - 20 °C

2.1: sodium hydride / mineral oil / 0.33 h

2.2: 0.5 h / 0 °C

3.1: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide / Inert atmosphere; Reflux

4.1: water; sodium hydroxide / methanol / 3 h / 20 °C

5.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Inert atmosphere

With water; sodium hydride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; potassium hydroxide; sodium hydroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In methanol; dichloromethane; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 1256964-50-7
3-iodo-2-methylpyrrolo[2,3-b]pyridine

: 1375278-66-2
(S)-N-(benzo[d][1,3]dioxol-5-yl)-N-methyl-2-(2-(2-methyl-3-vinyl-1H-pyrrolo[2,3-b]pyridin-1-yl)acetamido)-3-phenylpropanamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / mineral oil / 0.33 h

1.2: 0.5 h / 0 °C

2.1: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide / Inert atmosphere; Reflux

3.1: water; sodium hydroxide / methanol / 3 h / 20 °C

4.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Inert atmosphere

With water; sodium hydride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In methanol; dichloromethane; N,N-dimethyl-formamide; mineral oil;