2-Pteridinamine, 6-(3,4-dimethoxyphenyl)-4-(1-piperazinyl)-

Base Information

• Chemical Name: 2-Pteridinamine, 6-(3,4-dimethoxyphenyl)-4-(1-piperazinyl)-
• CAS No.: 278800-16-1
• Molecular Formula: C18H21N7O2
• Molecular Weight: 367.41
• DSSTox Substance ID: DTXSID80461079
• Wikidata: Q82285325
• Mol file: 278800-16-1.mol

Synonyms:278800-16-1;2-Pteridinamine, 6-(3,4-dimethoxyphenyl)-4-(1-piperazinyl)-;SCHEMBL4409272;DTXSID80461079;YLTIYCQHMPTGPB-UHFFFAOYSA-N;2-amino-4-piperazino-6-(3,4-dimethoxyphenyl)pteridine;2-amino-4-(piperazin-1-yl)-6-(3,4-dimethoxy-phenyl)pteridine

Chemical Property of 2-Pteridinamine, 6-(3,4-dimethoxyphenyl)-4-(1-piperazinyl)-

Chemical Property:

• XLogP3: 0.9
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 4
• Exact Mass: 367.17567294
• Heavy Atom Count: 27
• Complexity: 479

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=C(C=C(C=C1)C2=CN=C3C(=N2)C(=NC(=N3)N)N4CCNCC4)OC

Technology Process of 2-Pteridinamine, 6-(3,4-dimethoxyphenyl)-4-(1-piperazinyl)-

There total 1 articles about 2-Pteridinamine, 6-(3,4-dimethoxyphenyl)-4-(1-piperazinyl)- 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:

piperazine (110-85-0) + 2-amino-6-(3,4-dimethoxyphenyl)pterine → 2-amino-4-N-piperazinyl-6-(3,4-dimethoxyphenyl)-pteridine (278800-16-1)

Guidance literature:

With ammonium sulfate; toluene-4-sulfonic acid; 1,1,1,3,3,3-hexamethyl-disilazane; In toluene; at 120 ℃; for 24h;

DOI:10.1016/j.bmcl.2010.11.053

Reference yield:

2-amino-4-N-piperazinyl-6-(3,4-dimethoxyphenyl)-pteridine (278800-16-1) + m-chlorophenyl isocyanate (2909-38-8) → 2-amino-4-(N-3-chloro-phenyl-carbamoyl-piperazin-1-yl)-6-(3,4-dimethoxyphenyl)pteridine (923941-60-0)

Guidance literature:

In N,N-dimethyl-formamide; at 20 ℃; for 16h;

Reference yield:

2-amino-4-N-piperazinyl-6-(3,4-dimethoxyphenyl)-pteridine (278800-16-1) + benzoyl chloride (98-88-4) → C25H25N7O3 (850070-72-3)

Guidance literature:

With triethylamine; In dichloromethane; at 20 ℃; for 2h;

DOI:10.1016/j.bmcl.2010.11.053

upstream raw materials:

piperazine

Downstream raw materials:

2-amino-4-(N-3-chloro-phenyl-carbamoyl-piperazin-1-yl)-6-(3,4-dimethoxyphenyl)pteridine

C₂₆H₂₅N₉O₃

C₂₆H₂₈N₈O₃

C₂₅H₂₅N₇O₃

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