2-(2-(benzylthio)benzo[d]oxazol-5-yl)-1-(thiophen-2-ylmethyl)-1H-benzo[d]imidazole-5-carboxylic acid methyl ester

Base Information

• Chemical Name: 2-(2-(benzylthio)benzo[d]oxazol-5-yl)-1-(thiophen-2-ylmethyl)-1H-benzo[d]imidazole-5-carboxylic acid methyl ester
• CAS No.: 1354785-10-6
• Molecular Formula: C₂₈H₂₁N₃O₃S₂
• Molecular Weight: 511.625
• Mol file: 1354785-10-6.mol

Synonyms:

Chemical Property of 2-(2-(benzylthio)benzo[d]oxazol-5-yl)-1-(thiophen-2-ylmethyl)-1H-benzo[d]imidazole-5-carboxylic acid methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-(2-(benzylthio)benzo[d]oxazol-5-yl)-1-(thiophen-2-ylmethyl)-1H-benzo[d]imidazole-5-carboxylic acid methyl ester

There total 7 articles about 2-(2-(benzylthio)benzo[d]oxazol-5-yl)-1-(thiophen-2-ylmethyl)-1H-benzo[d]imidazole-5-carboxylic acid methyl ester 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:

C4H12B(1-)*C25H24N5O6S(1+) → 2-(2-(benzylthio)benzo[d]oxazol-5-yl)-1-(thiophen-2-ylmethyl)-1H-benzo[d]imidazole-5-carboxylic acid methyl ester (1354785-10-6)

Guidance literature:

Multi-step reaction with 5 steps

1: magnesium sulfate; trifluoroacetic acid / acetonitrile / 0.08 h / 140 °C / Microwave irradiation

2: palladium on activated charcoal; ammonium formate / methanol / 0.08 h / 90 °C / Microwave irradiation

3: acetonitrile / 0.08 h / 140 °C / Microwave irradiation

4: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 12 h / 20 °C

5: sodium methylate / 0.2 h / 90 °C / Microwave irradiation

With palladium on activated charcoal; ammonium formate; sodium methylate; magnesium sulfate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In methanol; N,N-dimethyl-formamide; acetonitrile;

DOI:10.1021/co200188g

Reference yield:

C4H12B(1-)*C25H22N5O5S(1+) → 2-(2-(benzylthio)benzo[d]oxazol-5-yl)-1-(thiophen-2-ylmethyl)-1H-benzo[d]imidazole-5-carboxylic acid methyl ester (1354785-10-6)

Guidance literature:

Multi-step reaction with 4 steps

1: palladium on activated charcoal; ammonium formate / methanol / 0.08 h / 90 °C / Microwave irradiation

2: acetonitrile / 0.08 h / 140 °C / Microwave irradiation

3: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 12 h / 20 °C

4: sodium methylate / 0.2 h / 90 °C / Microwave irradiation

With palladium on activated charcoal; ammonium formate; sodium methylate; N-ethyl-N,N-diisopropylamine; In methanol; N,N-dimethyl-formamide; acetonitrile;

DOI:10.1021/co200188g

Reference yield:

C4H12B(1-)*C26H22N5O3S2(1+) → 2-(2-(benzylthio)benzo[d]oxazol-5-yl)-1-(thiophen-2-ylmethyl)-1H-benzo[d]imidazole-5-carboxylic acid methyl ester (1354785-10-6)

Guidance literature:

Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 12 h / 20 °C

2: sodium methylate / 0.2 h / 90 °C / Microwave irradiation

With sodium methylate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide;

DOI:10.1021/co200188g

upstream raw materials:

methanol

3-nitro-4-hydroxybenzoic acid