(R)-7-bromo-5-methyl-2-((4-(methylsulphonyl)piperazin-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one

Base Information

• Chemical Name: (R)-7-bromo-5-methyl-2-((4-(methylsulphonyl)piperazin-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one
• CAS No.: 1610520-84-7
• Molecular Formula: C₁₄H₁₈BrN₃O₃S₂
• Molecular Weight: 420.351
• Mol file: 1610520-84-7.mol

Synonyms:(R)-7-bromo-5-methyl-2-((4-(methylsulphonyl)piperazin-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one

Chemical Property of (R)-7-bromo-5-methyl-2-((4-(methylsulphonyl)piperazin-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (R)-7-bromo-5-methyl-2-((4-(methylsulphonyl)piperazin-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one

There total 1 articles about (R)-7-bromo-5-methyl-2-((4-(methylsulphonyl)piperazin-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one 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:

2-bromothieno[3,2-c]pyridin-4(5H)-one (28948-60-9) → (R)-7-bromo-5-methyl-2-((4-(methylsulphonyl)piperazin-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one (1610520-84-7)

Guidance literature:

Multi-step reaction with 4 steps

1.1: n-butyllithium / tetrahydrofuran; hexane / 2.5 h / -78 - -60 °C / Inert atmosphere

1.2: 1 h / -60 - 20 °C / Inert atmosphere

2.1: N-Bromosuccinimide / tetrahydrofuran / 24 h / 20 °C

3.1: caesium carbonate / tetrahydrofuran / 0.33 h / 20 °C

3.2: 20 °C

4.1: acetic acid / methanol / 0.25 h / 20 °C

4.2: 1 h / 50 °C

With N-Bromosuccinimide; n-butyllithium; caesium carbonate; acetic acid; In tetrahydrofuran; methanol; hexane;

Reference yield: 92.0%

(R)-7-bromo-5-methyl-2-((4-(methylsulphonyl)piperazin-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one (1610520-84-7) + 3-hydroxyphenylboronic acid (87199-18-6) → 7-(3-hydroxyphenyl)-5-methyl-2-((4-(methylsulphonyl)piperazin-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one (1610518-21-2)

Guidance literature:

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate; In 1,2-dimethoxyethane; water; at 120 ℃; for 0.5h; Microwave irradiation;

Reference yield: 90.0%

4-((tert-butoxycarbonylamino)methyl)phenylboronic acid (489446-42-6) + (R)-7-bromo-5-methyl-2-((4-(methylsulphonyl)piperazin-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one (1610520-84-7) → tert-butyl 4-(5-methyl-2-((4-(methylsulphonyl)piperazin-1-yl)methyl)-4-oxo-4,5-dihydrothieno[3,2-c]pyridin-7-yl)benzylcarbamate (1610521-00-0)

Guidance literature:

With [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; potassium carbonate; In isopropyl alcohol; at 110 ℃; for 1h; Microwave irradiation;

upstream raw materials:

2-bromothieno[3,2-c]pyridin-4(5H)-one

Downstream raw materials:

5-methyl-2-((4-(methylsulphonyl)piperazin-1-yl)methyl)-7-(5-(1-phenylethoxy)pyridin-3-yl)thieno[3,2-c]pyridin-4(5H)-one hydrochloride

7-(5-(benzyloxy)pyridin-3-yl)-5-methyl-2-((4-(methylsulphonyl)piperazin-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one

tert-butyl 4-(5-methyl-2-((4-(methylsulphonyl)piperazin-1-yl)methyl)-4-oxo-4,5-dihydrothieno[3,2-c]pyridin-7-yl)benzylcarbamate

7-(3-isopropoxyphenyl)-5-methyl-2-((4-(methylsulphonyl)piperazin-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one