N-(4-chlorobenzyl)-2-[furan-2-ylmethyl-(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-amino]-acetamide

Base Information

• Chemical Name: N-(4-chlorobenzyl)-2-[furan-2-ylmethyl-(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-amino]-acetamide
• CAS No.: 1272663-07-6
• Molecular Formula: C₂₂H₂₄ClIN₄O₂
• Molecular Weight: 538.816
• Mol file: 1272663-07-6.mol

Synonyms:N-(4-chlorobenzyl)-2-[furan-2-ylmethyl-(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-amino]-acetamide

Chemical Property of N-(4-chlorobenzyl)-2-[furan-2-ylmethyl-(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-amino]-acetamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-(4-chlorobenzyl)-2-[furan-2-ylmethyl-(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-amino]-acetamide

There total 2 articles about N-(4-chlorobenzyl)-2-[furan-2-ylmethyl-(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-amino]-acetamide 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: 36.0%

formaldehyd (50-00-0,30525-89-4,61233-19-0) + furan-2-ylmethanamine (617-89-0) + 5-iodo-2-isopropyl-6-methyl-pyrimidin-4-ol (69696-38-4) + p-chlorobenzylisocyanide (39546-47-9) → N-(4-chlorobenzyl)-2-[furan-2-ylmethyl-(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-amino]-acetamide (1272663-07-6)

Guidance literature:

In methanol; at 60 ℃; for 72h;

DOI:10.1039/c0cc04164e

Reference yield:

2-isopropyl-6-methyl-4-pyrimidinol (2814-20-2) → N-(4-chlorobenzyl)-2-[furan-2-ylmethyl-(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-amino]-acetamide (1272663-07-6)

Guidance literature:

Multi-step reaction with 2 steps

1: iodine; potassium carbonate / tetrahydrofuran / Reflux

2: methanol / 72 h / 60 °C

With iodine; potassium carbonate; In tetrahydrofuran; methanol; 2: Ugi condensation;

DOI:10.1039/c0cc04164e

Reference yield: 68.0%

N-(4-chlorobenzyl)-2-[furan-2-ylmethyl-(5-iodo-2-isopropyl-6-methylpyrimidin-4-yl)-amino]-acetamide (1272663-07-6) → (E)-N-(4-chlorobenzyl)-2-[2-isopropyl-4-methyl-5-(3-oxopropenyl)-pyrrolo[2,3-d]pyrimidin-7-yl]-acetamide (1272662-53-9)

Guidance literature:

With bis-triphenylphosphine-palladium(II) chloride; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 130 ℃; for 0.333333h; under 9750.98 Torr; Microwave irradiation;

DOI:10.1039/c0cc04164e

upstream raw materials:

formaldehyd

furan-2-ylmethanamine

5-iodo-2-isopropyl-6-methyl-pyrimidin-4-ol

p-chlorobenzylisocyanide

Downstream raw materials:

(E)-N-(4-chlorobenzyl)-2-[2-isopropyl-4-methyl-5-(3-oxopropenyl)-pyrrolo[2,3-d]pyrimidin-7-yl]-acetamide