N-[tert-butylcarbamoyl-(2-iodo-phenyl)-methyl]-3-methoxy-N-pyrrolidin-3-ylmethyl-benzamide

Base Information

• Chemical Name: N-[tert-butylcarbamoyl-(2-iodo-phenyl)-methyl]-3-methoxy-N-pyrrolidin-3-ylmethyl-benzamide
• CAS No.: 849590-01-8
• Molecular Formula: C₂₅H₃₂IN₃O₃
• Molecular Weight: 549.452

Synonyms:N-[tert-butylcarbamoyl-(2-iodo-phenyl)-methyl]-3-methoxy-N-pyrrolidin-3-ylmethyl-benzamide

Chemical Property of N-[tert-butylcarbamoyl-(2-iodo-phenyl)-methyl]-3-methoxy-N-pyrrolidin-3-ylmethyl-benzamide

Chemical Property:

Purity/Quality:

98% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-[tert-butylcarbamoyl-(2-iodo-phenyl)-methyl]-3-methoxy-N-pyrrolidin-3-ylmethyl-benzamide

There total 3 articles about N-[tert-butylcarbamoyl-(2-iodo-phenyl)-methyl]-3-methoxy-N-pyrrolidin-3-ylmethyl-benzamide 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:

3-{[[tert-butylcarbamoyl-(2-iodo-phenyl)-methyl]-(3-methoxy-benzoyl)-amino]-methyl}-pyrrolidine-1-carboxylic acid tert-butyl ester → N-[tert-butylcarbamoyl-(2-iodo-phenyl)-methyl]-3-methoxy-N-pyrrolidin-3-ylmethyl-benzamide (849590-01-8)

Guidance literature:

With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 6h;

DOI:10.1016/j.tetlet.2005.01.063

Reference yield:

2-iodobenzaldehyde (26260-02-6) → N-[tert-butylcarbamoyl-(2-iodo-phenyl)-methyl]-3-methoxy-N-pyrrolidin-3-ylmethyl-benzamide (849590-01-8)

Guidance literature:

Multi-step reaction with 2 steps

1: methanol / 18 h / 20 °C

2: aq. HCl / dioxane / 6 h / 20 °C

With hydrogenchloride; In 1,4-dioxane; methanol; 1: Ugi reaction;

DOI:10.1016/j.tetlet.2005.01.063

Reference yield:

tert-butyl 3-(aminomethyl)pyrrolidine-1-carboxylate (270912-72-6) → N-[tert-butylcarbamoyl-(2-iodo-phenyl)-methyl]-3-methoxy-N-pyrrolidin-3-ylmethyl-benzamide (849590-01-8)

Guidance literature:

Multi-step reaction with 2 steps

1: methanol / 18 h / 20 °C

2: aq. HCl / dioxane / 6 h / 20 °C

With hydrogenchloride; In 1,4-dioxane; methanol; 1: Ugi reaction;

DOI:10.1016/j.tetlet.2005.01.063

upstream raw materials:

2-iodobenzaldehyde

tert-butyl 3-(aminomethyl)pyrrolidine-1-carboxylate

Post a RFQ

Cas No.:

Product Name:

Quantity:

Please select Metric Ton KG G Pound L ML

Email:

Company name:

Valid Period:

Detailed Requirements:

• Sample
• MOQ
• GMP
• FDA
• Price
  FOB CIF CFR EXW
• Urgent purchase

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

Remove

Submit

1

What can I do for you?
Get Best Price

Get Best Price for 849590-01-8 N-[tert-butylcarbamoyl-(2-iodo-phenyl)-methyl]-3-methoxy-N-pyrrolidin-3-ylmethyl-benzamide

Send

Send

Metric Ton KG G Pound L ML

Send

Send