ChemicalBook--->CAS DataBase List--->2565-47-1

2565-47-1

2565-47-1 Structure

2565-47-1 Structure
IdentificationBack Directory
[Name]

N-METHYLBARBITURIC ACID
[CAS]

2565-47-1
[Synonyms]

Alogliptin-17
N-Methylbarituric Acid
alogliptina impurity 5
3-METHYLBARBITURIC ACID
N-METHYLBARBITURIC ACID
1-methylbarbituric acid
N-Methylbarituric Acid 1
1-Methyl-pyrimidine-2,4,6-trione
1-Methylpyrimidine-2,4,6(1H,3H,5H)
1-methyl-1,3-diazinane-2,4,6-trione
1-Methyl-2,4,6-Trihydroxy-Pyrimidine
1-Methylpyrimidine-2,4,6(1H,3H,5H)-trione
2,4,6(1H,3H,5H)-Pyrimidinetrione,1-methyl-
[EINECS(EC#)]

219-894-0
[Molecular Formula]

C5H6N2O3
[MDL Number]

MFCD00038667
[MOL File]

2565-47-1.mol
[Molecular Weight]

142.11
Chemical PropertiesBack Directory
[Melting point ]

132 °C
[density ]

1.379±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

DMSO (Sparingly), Methanol (Slightly)
[form ]

Solid
[pka]

pK1:4.35(+1) (25°C)
[color ]

White to Off-White
[InChI]

InChI=1S/C5H6N2O3/c1-7-4(9)2-3(8)6-5(7)10/h2H2,1H3,(H,6,8,10)
[InChIKey]

DCGGMHIZEAHUJL-UHFFFAOYSA-N
[SMILES]

C1(=O)N(C)C(=O)CC(=O)N1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933599590
Hazard InformationBack Directory
[Uses]

1-Methylbarbituric Acid is an impurity of Trelagliptin. Trelagliptin (Zafatek) is a pharmaceutical drug used for the treatment of type 2 diabetes.
[Synthesis]

Malonic acid

141-82-2

Methylurea

598-50-5

N-METHYLBARBITURIC ACID

2565-47-1

Acetic anhydride (130 mL, 1.37 mol) was slowly added dropwise to 180 mL of acetic acid solution containing malonic acid (80 g, 0.79 mol) and N-methylurea (50 g, 0.68 mol) at 70 °C. After the dropwise addition was completed, the reaction mixture was warmed up to 90 °C with continuous stirring for 3 hours. After completion of the reaction, the mixture was cooled to room temperature. The solvent was removed by distillation under reduced pressure and the resulting residue was treated with 350 mL of ethanol to precipitate a pale yellow solid. The solid was purified by recrystallization from ethanol to give 63.1 g of 1-methylpyrimidine-2,4,6(1H,3H,5H)-trione as a final crystalline solid (yield: 65.8%). The melting point was measured to be 131.2-133.1 °C (literature value: 130-131.5 °C).

[References]

[1] Journal of Heterocyclic Chemistry, 2014, vol. 51, # 3, p. 594 - 597
[2] Journal of Medicinal Chemistry, 1989, vol. 32, # 6, p. 1231 - 1237
[3] Patent: WO2009/73210, 2009, A1. Location in patent: Page/Page column 76
[4] Patent: WO2006/133261, 2006, A2. Location in patent: Page/Page column 30
[5] Patent: WO2007/143705, 2007, A2. Location in patent: Page/Page column 23
Spectrum DetailBack Directory
[Spectrum Detail]

N-METHYLBARBITURIC ACID(2565-47-1)MS
N-METHYLBARBITURIC ACID(2565-47-1)IR1
N-METHYLBARBITURIC ACID(2565-47-1)IR2
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