1-(4-bromo-5-methylthiophen-2-yl)-N-(4-chlorobenzyl)-N-(pyridin-3-ylmethyl)methanamine

Base Information

• Chemical Name: 1-(4-bromo-5-methylthiophen-2-yl)-N-(4-chlorobenzyl)-N-(pyridin-3-ylmethyl)methanamine
• CAS No.: 1437786-93-0
• Molecular Formula: C₁₉H₁₈BrClN₂S
• Molecular Weight: 421.788

Synonyms:1-(4-bromo-5-methylthiophen-2-yl)-N-(4-chlorobenzyl)-N-(pyridin-3-ylmethyl)methanamine

Chemical Property of 1-(4-bromo-5-methylthiophen-2-yl)-N-(4-chlorobenzyl)-N-(pyridin-3-ylmethyl)methanamine

Chemical Property:

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Technology Process of 1-(4-bromo-5-methylthiophen-2-yl)-N-(4-chlorobenzyl)-N-(pyridin-3-ylmethyl)methanamine

There total 3 articles about 1-(4-bromo-5-methylthiophen-2-yl)-N-(4-chlorobenzyl)-N-(pyridin-3-ylmethyl)methanamine 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: 54.0%

3-bromo-2-methyl-5-thiophenecarboxyaldehyde (29421-75-8) + [(4-chlorophenyl)methyl](3-pyridinylmethyl)amine (212392-65-9) → 1-(4-bromo-5-methylthiophen-2-yl)-N-(4-chlorobenzyl)-N-(pyridin-3-ylmethyl)methanamine (1437786-93-0)

Guidance literature:

With sodium cyanoborohydride; acetic acid; In ethanol; dichloromethane; at 120 ℃; for 0.166667h; Microwave irradiation;

DOI:10.1021/jm400458q

Reference yield:

3-pyridinecarboxaldehyde (500-22-1) → 1-(4-bromo-5-methylthiophen-2-yl)-N-(4-chlorobenzyl)-N-(pyridin-3-ylmethyl)methanamine (1437786-93-0)

Guidance literature:

Multi-step reaction with 2 steps

1.1: 0.08 h / 20 °C

1.2: 16 h / 20 °C

2.1: sodium cyanoborohydride; acetic acid / dichloromethane; ethanol / 0.17 h / 120 °C / Microwave irradiation

With sodium cyanoborohydride; acetic acid; In ethanol; dichloromethane;

DOI:10.1021/jm400458q

Reference yield:

4-chlorobenzylamine (104-86-9) → 1-(4-bromo-5-methylthiophen-2-yl)-N-(4-chlorobenzyl)-N-(pyridin-3-ylmethyl)methanamine (1437786-93-0)

Guidance literature:

Multi-step reaction with 2 steps

1.1: 0.08 h / 20 °C

1.2: 16 h / 20 °C

2.1: sodium cyanoborohydride; acetic acid / dichloromethane; ethanol / 0.17 h / 120 °C / Microwave irradiation

With sodium cyanoborohydride; acetic acid; In ethanol; dichloromethane;

DOI:10.1021/jm400458q

upstream raw materials:

3-bromo-2-methyl-5-thiophenecarboxyaldehyde

[(4-chlorophenyl)methyl](3-pyridinylmethyl)amine

4-chlorobenzylamine

3-pyridinecarboxaldehyde

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