Cas no 861031-56-3 (2-Amino-4-morpholin-4-yl-pyrimidine)

2-Amino-4-morpholin-4-yl-pyrimidine structure
861031-56-3 structure
Product Name:2-Amino-4-morpholin-4-yl-pyrimidine
CAS No:861031-56-3
MF:C8H12N4O
MW:180.207080841064
MDL:MFCD11520888
CID:838704
Update Time:2024-10-26

2-Amino-4-morpholin-4-yl-pyrimidine Chemical and Physical Properties

Names and Identifiers

    • 2-Amino-4-morpholin-4-yl-pyrimidine
    • 4-morpholin-4-ylpyrimidin-2-amine
    • 4-morpholinopyrimidin-2-amine
    • 4-(morpholin-4-yl)pyrimidin-2-amine
    • UMUSFEOPXQLLAG-UHFFFAOYSA-N
    • 4-(2-Amino-4-pyrimidyl)morpholine
    • AB0027056
    • W8844
    • ST24027733
    • 4-(4-Morpholinyl)-2-pyrimidinamine (ACI)
    • Pyrimidine, 2-amino-4-(4-morpholinyl)- (4CI)
    • [4-(Morpholin-4-yl)pyrimidin-2-yl]amine
    • MDL： MFCD11520888
    • Inchi： 1S/C8H12N4O/c9-8-10-2-1-7(11-8)12-3-5-13-6-4-12/h1-2H,3-6H2,(H2,9,10,11)
    • InChI Key： UMUSFEOPXQLLAG-UHFFFAOYSA-N
    • SMILES： N1C(N)=NC(N2CCOCC2)=CC=1

Computed Properties

  • Exact Mass: 180.10100
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 1
  • Complexity: 160
  • Topological Polar Surface Area: 64.3

Experimental Properties

  • PSA: 64.27000
  • LogP: 0.54160

2-Amino-4-morpholin-4-yl-pyrimidine Security Information

2-Amino-4-morpholin-4-yl-pyrimidine Customs Data

  • HS CODE：2934999090
  • Customs Data：

    China Customs Code:

    2934999090

    Overview:

    2934999090. Other heterocyclic compounds. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

2-Amino-4-morpholin-4-yl-pyrimidine Pricemore >>

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2-Amino-4-morpholin-4-yl-pyrimidine Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Diisopropylethylamine Solvents: Acetonitrile ;  4 h, reflux
Reference
Design, synthesis and biological evaluation of 2-methyl-(1,1'-biphenyl)-pyrimidine conjugates
Chen, An; et al, Bioorganic & Medicinal Chemistry Letters, 2020, 30(16),

Production Method 2

Reaction Conditions
1.1 Reagents: Sodium ethoxide Solvents: Methanol ;  6 h, 90 °C
2.1 Reagents: Phosphorus oxychloride ;  rt; 8 h, 110 °C
2.2 Reagents: Sodium carbonate Solvents: Water ;  pH 10 - 11, 0 °C
3.1 Reagents: Triethylamine Solvents: Tetrahydrofuran ;  16 h, 80 °C
3.2 Reagents: Sodium carbonate Solvents: Water ;  pH 9 - 10
4.1 Reagents: Zinc Solvents: Acetic acid ;  18 h, 120 °C; 120 °C → rt
4.2 Reagents: Sodium carbonate Solvents: Water ;  pH 8 - 9
Reference
An Efficient Synthetic Method for the Synthesis of Novel Pyrimido[1,2-a]Pyrimidine-3-Carboxylates: Comparison of Irradiation and Conventional Conditions
Bayramoglu, Duygu; et al, Polycyclic Aromatic Compounds, 2022, 42(8), 4948-4964

Production Method 3

Reaction Conditions
1.1 Reagents: Zinc Solvents: Acetic acid ;  18 h, 120 °C; 120 °C → rt
1.2 Reagents: Sodium carbonate Solvents: Water ;  pH 8 - 9
Reference
An Efficient Synthetic Method for the Synthesis of Novel Pyrimido[1,2-a]Pyrimidine-3-Carboxylates: Comparison of Irradiation and Conventional Conditions
Bayramoglu, Duygu; et al, Polycyclic Aromatic Compounds, 2022, 42(8), 4948-4964

Production Method 4

Reaction Conditions
1.1 Reagents: Triethylamine Solvents: Tetrahydrofuran ;  16 h, 80 °C
1.2 Reagents: Sodium carbonate Solvents: Water ;  pH 9 - 10
2.1 Reagents: Zinc Solvents: Acetic acid ;  18 h, 120 °C; 120 °C → rt
2.2 Reagents: Sodium carbonate Solvents: Water ;  pH 8 - 9
Reference
An Efficient Synthetic Method for the Synthesis of Novel Pyrimido[1,2-a]Pyrimidine-3-Carboxylates: Comparison of Irradiation and Conventional Conditions
Bayramoglu, Duygu; et al, Polycyclic Aromatic Compounds, 2022, 42(8), 4948-4964

Production Method 5

Reaction Conditions
1.1 Reagents: Phosphorus oxychloride ;  rt; 8 h, 110 °C
1.2 Reagents: Sodium carbonate Solvents: Water ;  pH 10 - 11, 0 °C
2.1 Reagents: Triethylamine Solvents: Tetrahydrofuran ;  16 h, 80 °C
2.2 Reagents: Sodium carbonate Solvents: Water ;  pH 9 - 10
3.1 Reagents: Zinc Solvents: Acetic acid ;  18 h, 120 °C; 120 °C → rt
3.2 Reagents: Sodium carbonate Solvents: Water ;  pH 8 - 9
Reference
An Efficient Synthetic Method for the Synthesis of Novel Pyrimido[1,2-a]Pyrimidine-3-Carboxylates: Comparison of Irradiation and Conventional Conditions
Bayramoglu, Duygu; et al, Polycyclic Aromatic Compounds, 2022, 42(8), 4948-4964

2-Amino-4-morpholin-4-yl-pyrimidine Raw materials

2-Amino-4-morpholin-4-yl-pyrimidine Preparation Products

2-Amino-4-morpholin-4-yl-pyrimidine Related Literature

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