N-methyl-N-<3-<(4-amino-6,7-dimethoxy-2-quinazolinyl)methylamino>propyl>-3-methoxybenzenecarboxamide

Base Information

• Chemical Name: N-methyl-N-<3-<(4-amino-6,7-dimethoxy-2-quinazolinyl)methylamino>propyl>-3-methoxybenzenecarboxamide
• CAS No.: 98902-40-0
• Molecular Formula: C₂₃H₂₉N₅O₄
• Molecular Weight: 439.514
• Mol file: 98902-40-0.mol

Synonyms:N-methyl-N-<3-<(4-amino-6,7-dimethoxy-2-quinazolinyl)methylamino>propyl>-3-methoxybenzenecarboxamide

Chemical Property of N-methyl-N-<3-<(4-amino-6,7-dimethoxy-2-quinazolinyl)methylamino>propyl>-3-methoxybenzenecarboxamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-methyl-N-<3-<(4-amino-6,7-dimethoxy-2-quinazolinyl)methylamino>propyl>-3-methoxybenzenecarboxamide

There total 3 articles about N-methyl-N-<3-<(4-amino-6,7-dimethoxy-2-quinazolinyl)methylamino>propyl>-3-methoxybenzenecarboxamide 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:

N1,N2-dimethyl-N1-(phenylmethyl)-1,3-propanediamine (60630-68-4) → N-methyl-N-<3-<(4-amino-6,7-dimethoxy-2-quinazolinyl)methylamino>propyl>-3-methoxybenzenecarboxamide (98902-40-0)

Guidance literature:

Multi-step reaction with 3 steps

1: 70 percent / pyridine / 0.5 h / 130 °C

2: 85 percent / H₂, HCl / 5percent Pd/C / ethanol; methanol / 80 °C / 14480.1 Torr

3: NaOH / H₂O; CHCl₃ / 1 h / Ambient temperature

With hydrogenchloride; sodium hydroxide; hydrogen; palladium on activated charcoal; In pyridine; methanol; ethanol; chloroform; water;

DOI:10.1021/jm00151a003

Reference yield:

N1,N2-dimethyl-N2-(phenylmethyl)-N1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-1,3-propanediamine (65189-24-4) → N-methyl-N-<3-<(4-amino-6,7-dimethoxy-2-quinazolinyl)methylamino>propyl>-3-methoxybenzenecarboxamide (98902-40-0)

Guidance literature:

Multi-step reaction with 2 steps

1: 85 percent / H₂, HCl / 5percent Pd/C / ethanol; methanol / 80 °C / 14480.1 Torr

2: NaOH / H₂O; CHCl₃ / 1 h / Ambient temperature

With hydrogenchloride; sodium hydroxide; hydrogen; palladium on activated charcoal; In methanol; ethanol; chloroform; water;

DOI:10.1021/jm00151a003

Reference yield:

m-anisoyl chloride (1711-05-3) + N1,N2-dimethyl-N1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-1,3-propanediamine hydrochloride (65189-25-5) → N-methyl-N-<3-<(4-amino-6,7-dimethoxy-2-quinazolinyl)methylamino>propyl>-3-methoxybenzenecarboxamide (98902-40-0)

Guidance literature:

With sodium hydroxide; In chloroform; water; for 1h; Ambient temperature;

DOI:10.1021/jm00151a003

upstream raw materials:

m-anisoyl chloride

N¹,N²-dimethyl-N¹-(4-amino-6,7-dimethoxy-2-quinazolinyl)-1,3-propanediamine hydrochloride

N¹,N²-dimethyl-N¹-(phenylmethyl)-1,3-propanediamine

N¹,N²-dimethyl-N²-(phenylmethyl)-N¹-(4-amino-6,7-dimethoxy-2-quinazolinyl)-1,3-propanediamine