N-[(3-bromobenzylcarbamoyl)methyl]-3-(7-bromo-3H-indol-3-yl)propionamide

Base Information

Chemical Name:N-[(3-bromobenzylcarbamoyl)methyl]-3-(7-bromo-3H-indol-3-yl)propionamide
CAS No.:210569-79-2
Molecular Formula:C₂₀H₁₉Br₂N₃O₂
Molecular Weight:493.198
Hs Code.:

Synonyms:N-[(3-bromobenzylcarbamoyl)methyl]-3-(7-bromo-3H-indol-3-yl)propionamide

Suppliers and Price of N-[(3-bromobenzylcarbamoyl)methyl]-3-(7-bromo-3H-indol-3-yl)propionamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-[(3-bromobenzylcarbamoyl)methyl]-3-(7-bromo-3H-indol-3-yl)propionamide

Chemical Property:

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Technology Process of N-[(3-bromobenzylcarbamoyl)methyl]-3-(7-bromo-3H-indol-3-yl)propionamide

There total 8 articles about N-[(3-bromobenzylcarbamoyl)methyl]-3-(7-bromo-3H-indol-3-yl)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: 38.0%

: 39959-54-1
3-bromobenzylamine hydrochloride

: 210569-72-5
[3-(7-bromo-3H-indol-3-yl)propionylamino]acetic acid

: 210569-79-2
N-[(3-bromobenzylcarbamoyl)methyl]-3-(7-bromo-3H-indol-3-yl)propionamide

Guidance literature:: With benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 15h;
DOI:10.3987/COM-99-8514

Reference yield:

: 115666-21-2
7-bromo-1 H-indole-3-carbaldehyde

: 210569-79-2
N-[(3-bromobenzylcarbamoyl)methyl]-3-(7-bromo-3H-indol-3-yl)propionamide

Guidance literature:: Multi-step reaction with 6 steps

1: 60 percent / piperidine / pyridine / 24 h / 50 °C

2: 40 percent / BiCl₃; NaBH₄ / aq. ethanol / 4 h / 0 °C

3: 98 percent / NaOH / methanol; H₂O / 4 h / 20 °C

4: 58 percent / N(C₂H₅)3; HOBT; EDC / dimethylformamide / 8 h / 20 °C

5: 84 percent / NaOH; H₂O / methanol / 5 h / 20 °C

6: 38 percent / N(C₂H₅)3; EDC; HOBT / dimethylformamide / 15 h / 20 °C

With piperidine; bismuth(III) chloride; sodium hydroxide; sodium tetrahydroborate; water; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; In pyridine; methanol; ethanol; water; N,N-dimethyl-formamide; 1: Alkylation / 2: Reduction / 3: Hydrolysis / 4: Acylation / 5: Hydrolysis / 6: Acylation;
DOI:10.3987/COM-99-8514

Reference yield:

: 210569-70-3
3-(7-bromo-3H-indol-3-yl)propionic acid

: 210569-79-2
N-[(3-bromobenzylcarbamoyl)methyl]-3-(7-bromo-3H-indol-3-yl)propionamide

Guidance literature:: Multi-step reaction with 3 steps

1: 58 percent / N(C₂H₅)3; HOBT; EDC / dimethylformamide / 8 h / 20 °C

2: 84 percent / NaOH; H₂O / methanol / 5 h / 20 °C

3: 38 percent / N(C₂H₅)3; EDC; HOBT / dimethylformamide / 15 h / 20 °C

With sodium hydroxide; water; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; In methanol; N,N-dimethyl-formamide; 1: Acylation / 2: Hydrolysis / 3: Acylation;
DOI:10.3987/COM-99-8514