N-METHYLBARBITURIC ACID

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Company Name: Nanjing Chalf-Pharm Technology Co., Ltd.  Gold
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N-METHYLBARBITURIC ACID manufacturers

N-METHYLBARBITURIC ACID Basic information
Product Name:N-METHYLBARBITURIC ACID
Synonyms:N-METHYLBARBITURIC ACID;1-Methyl-2,4,6-Trihydroxy-Pyrimidine;1-Methylpyrimidine-2,4,6(1H,3H,5H)-trione;3-METHYLBARBITURIC ACID;Alogliptin-17;N-Methylbarituric Acid 1;1-methyl-1,3-diazinane-2,4,6-trione;1-Methylpyrimidine-2,4,6(1H,3H,5H)
CAS:2565-47-1
MF:C5H6N2O3
MW:142.11
EINECS:219-894-0
Product Categories:
Mol File:2565-47-1.mol
N-METHYLBARBITURIC ACID Structure
N-METHYLBARBITURIC ACID Chemical Properties
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
pkapK1:4.35(+1) (25°C)
color White to Off-White
InChIInChI=1S/C5H6N2O3/c1-7-4(9)2-3(8)6-5(7)10/h2H2,1H3,(H,6,8,10)
InChIKeyDCGGMHIZEAHUJL-UHFFFAOYSA-N
SMILESC1(=O)N(C)C(=O)CC(=O)N1
Safety Information
HS Code 2933599590
MSDS Information
N-METHYLBARBITURIC ACID Usage And Synthesis
Uses1-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
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