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65996-50-1

65996-50-1 Structure

65996-50-1 Structure
IdentificationBack Directory
[Name]

1,5-Dihydropyrrolo[3,2-a]pyrimidine-2,4-dion
[CAS]

65996-50-1
[Synonyms]

65996-50-1
1,5-dihydro-pyrrolo[3,2-a]pyri
5H-Pyrrolo[3,2-d]pyriMidine-2,4-diol
1-Pyrrolo[3,2-d]pyrimidine-2,4(3H,5H)-dione
1,5-DIHYDROPYRROLO[3,2-A]PYRIMIDINE-2,4-DION
1,5-DIHYDRO-PYRROLO[3,2-A]PYRIMIDINE-2,4-DIONE
1,5-DIHYDRO-PYRROLO[3,2-D]PYRIMIDINE-2,4-DIONE
1H,2H,3H,4H,5H-pyrrolo[3,2-d]pyriMidine-2,4-dione
1,5-Dihydro-2H-pyrrolo[3,2-d]pyrimidine-2,4(3H)-dione
[Molecular Formula]

C6H5N3O2
[MDL Number]

MFCD08059275
[MOL File]

65996-50-1.mol
[Molecular Weight]

151.12
Chemical PropertiesBack Directory
[Melting point ]

>360 °C(Solv: water (7732-18-5))
[density ]

1.516±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[form ]

powder to crystal
[pka]

11.32±0.20(Predicted)
[color ]

White to Light yellow to Light orange
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22
[HS Code ]

2933.59.8000
Hazard InformationBack Directory
[Uses]

1,5-Dihydropyrrolo[3,2-a]pyrimidine-2,4-dion is used for the preparation of pyrazolopyrimidine derivatives or analogs thereof as CCR4 function modulators.
[Synthesis]

(E)-6-(2-(dimethylamino)vinyl)-5-nityopyrimidine-2,4-diol

116705-41-0

1,5-Dihydropyrrolo[3,2-a]pyrimidine-2,4-dion

65996-50-1

General procedure for the synthesis of 1H-pyrrolo[2,3-d]pyrimidine-2,4(3H,7H)-dione from (E)-6-(2-(dimethylamino)vinyl)-5-nitropyrimidine-2,4(1H,3H)-dione: (E)-6-(2-(dimethylamino)vinyl)-5-nitropyrimidine-2,4(1H,3H)-dione (1 g, 4.4 mmol) was dissolved in freshly prepared glacial acetic acid (50 mL) and stirred to form a slurry. Under stirring, zinc powder (stabilized, 1g per batch, 2g total) was added in two batches with an interval of 1 hour. The reaction mixture was stirred overnight and the color of the slurry was observed to change gradually from yellow to light yellow to off-white. After completion of the reaction, the mixture was filtered and the filtrate was concentrated under vacuum to obtain a brown slurry. The product was separated from the brown slurry by ethanol precipitation to give a white solid (0.6 g, 89.8% yield). The spectral data of the product were consistent with those reported in the literature.1H NMR (400 MHz, DMSO-d6): δ 5.82-5.83 (t, 1H, J=2.28 Hz), 7.12-7.13 (t, 1H, J=2.72 Hz, J=2.96 Hz), 10.57 (s, 1H), 10.74 (s, 1H), 11.82 (s. 1H).13C NMR (400 MHz, DMSO-d6): δ 96.5, 110.9, 127.4, 135.1, 152.0, 156.3.

[References]

[1] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 15, p. 4354 - 4363
[2] Patent: US2016/257696, 2016, A1. Location in patent: Paragraph 0068
[3] Patent: WO2009/62258, 2009, A1. Location in patent: Page/Page column 98
[4] ChemMedChem, 2018, vol. 13, # 2, p. 178 - 185
Spectrum DetailBack Directory
[Spectrum Detail]

1,5-Dihydropyrrolo[3,2-a]pyrimidine-2,4-dion(65996-50-1)1HNMR
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