N-<4-<(2,4-Diamino-6-pteridinyl)methyl>methylaminobenzoyl>-β-(4-bromphenyl)glutaminsaeure

Base Information

• Chemical Name: N-<4-<(2,4-Diamino-6-pteridinyl)methyl>methylaminobenzoyl>-β-(4-bromphenyl)glutaminsaeure
• CAS No.: 136451-07-5
• Molecular Formula: C₂₆H₂₅BrN₈O₅
• Molecular Weight: 609.439
• Mol file: 136451-07-5.mol

Synonyms:N-<4-<(2,4-Diamino-6-pteridinyl)methyl>methylaminobenzoyl>-β-(4-bromphenyl)glutaminsaeure

Chemical Property of N-<4-<(2,4-Diamino-6-pteridinyl)methyl>methylaminobenzoyl>-β-(4-bromphenyl)glutaminsaeure

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-<4-<(2,4-Diamino-6-pteridinyl)methyl>methylaminobenzoyl>-β-(4-bromphenyl)glutaminsaeure

There total 4 articles about N-<4-<(2,4-Diamino-6-pteridinyl)methyl>methylaminobenzoyl>-β-(4-bromphenyl)glutaminsaeure 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: 92.0%

Diethyl-N-<4-<(2,4-diamino-6-pteridinyl)methyl>-N-methylaminobenzoyl>-β-(4-bromphenyl)glutamat (136451-03-1) → N-<4-<(2,4-Diamino-6-pteridinyl)methyl>methylaminobenzoyl>-β-(4-bromphenyl)glutaminsaeure (136451-07-5)

Guidance literature:

With sodium hydroxide; In ethanol; for 3h; Ambient temperature;

DOI:10.1002/ardp.2503240808

Reference yield:

6-bromomethyl-pteridine-2,4-diamine (59368-16-0) → N-<4-<(2,4-Diamino-6-pteridinyl)methyl>methylaminobenzoyl>-β-(4-bromphenyl)glutaminsaeure (136451-07-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 76 percent / N,N-dimethyl-acetamide / 1.) 50 to 55 deg C, 4 h 2.) 25 deg C, 17 h

2: 92 percent / N aq. NaOH / ethanol / 3 h / Ambient temperature

With sodium hydroxide; In ethanol; N,N-dimethyl acetamide;

DOI:10.1002/ardp.2503240808

Reference yield:

4-(N-Methyl-N-tosyl)aminobenzoylchlorid (16879-69-9) → N-<4-<(2,4-Diamino-6-pteridinyl)methyl>methylaminobenzoyl>-β-(4-bromphenyl)glutaminsaeure (136451-07-5)

Guidance literature:

Multi-step reaction with 3 steps

1: 74 percent / KHCO₃ / CH₂Cl₂; H₂O / 12 h / Ambient temperature

2: 76 percent / N,N-dimethyl-acetamide / 1.) 50 to 55 deg C, 4 h 2.) 25 deg C, 17 h

3: 92 percent / N aq. NaOH / ethanol / 3 h / Ambient temperature

With sodium hydroxide; potassium hydrogencarbonate; In ethanol; dichloromethane; N,N-dimethyl acetamide; water;

DOI:10.1002/ardp.2503240808

upstream raw materials:

Diethyl-N-<4-<(2,4-diamino-6-pteridinyl)methyl>-N-methylaminobenzoyl>-β-(4-bromphenyl)glutamat

6-bromomethyl-pteridine-2,4-diamine

4-(N-Methyl-N-tosyl)aminobenzoylchlorid

Diethyl-N-<4-(N-methyl)aminobenzoyl>-β-(4-bromphenyl)glutamat