ChemicalBook--->CAS DataBase List--->635698-34-9

635698-34-9

635698-34-9 Structure

635698-34-9 Structure
IdentificationBack Directory
[Name]

6-benzyl-6,7-dihydro-1H-pyrrolo[3,4-d]pyrimidine-2,4(3H,5H)-dione
[CAS]

635698-34-9
[Synonyms]

5H)-dione
6-benzyl-6
6-Benzyl-6,7-dihydro-5H-pyrrolo[3,4-d]pyriMidine-2,4-diol
6-benzyl-5,7-dihydro-1H-pyrrolo[3,4-d]pyrimidine-2,4-dione
6-benzyl-5,7-dihydro-1H-pyrrolo[3,4-e]pyrimidine-2,4-dione
6-Benzyl-6,7-dihydro-1H-pyrrolo[3,4-d]pyrimidine-2,4(3H,5H)
6-Benzyl-1,5,6,7-tetrahydro-pyrrolo[3,4-d]pyrimidine-2,4-dione
6-benzyl-1H,2H,3H,4H,5H,6H,7H-pyrrolo[3,4-d]pyriMidine-2,4-dione
6-benzyl-6,7-dihydro-1H-pyrrolo[3,4-d]pyrimidine-2,4(3H,5H)-dione
6-(phenylmethyl)-5,7-dihydro-1H-pyrrolo[3,4-d]pyrimidine-2,4-dione
6-Benzyl-1,5,6,7-tetrahydro-2H-pyrrolo[3,4-d]pyrimidine-2,4(3H)-dione
1H-Pyrrolo[3,4-d]pyriMidine-2,4(3H,5H)-dione, 6,7-dihydro-6-(phenylMethyl)-
[EINECS(EC#)]

1533716-785-6
[Molecular Formula]

C13H13N3O2
[MDL Number]

MFCD10699254
[MOL File]

635698-34-9.mol
[Molecular Weight]

243.26
Chemical PropertiesBack Directory
[density ]

1.37±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

10.07±0.20(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

6-benzyl-6,7-dihydro-1H-pyrrolo[3,4-d]pyrimidine-2,4(3H,5H)-dione(635698-34-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

ethyl 1-benzyl-4-oxo-pyrrolidine-3-carboxylate

1027-35-6

Urea

57-13-6

6-benzyl-6,7-dihydro-1H-pyrrolo[3,4-d]pyrimidine-2,4(3H,5H)-dione

635698-34-9

Ethyl 1-benzyl-4-keto-3-pyrrolidinecarboxylate (9.23 g, 0.0372 mol) was dissolved in ethanol (170 mL), to which a methanolic solution of urea (11.2 g, 0.186 mol) and sodium methanolate (~28%, 25 g) was added. The reaction mixture was stirred under reflux conditions for 24 hours. Upon completion of the reaction, the reaction mixture was mixed with water (100 mL) and stirring was continued at room temperature. Subsequently, dilute hydrochloric acid (~1 mol/L, 100 mL) was added slowly and dropwise to the reaction mixture. The precipitated solid was collected by filtration and washed with water (100 mL). Finally, the resulting solid was dried under reduced pressure to afford 6-benzyl-6,7-dihydro-1H-pyrrolo[3,4-D]pyrimidine-2,4(3H,5H)-dione (3.93 g, 43% yield).

[References]

[1] Patent: EP1552842, 2005, A1. Location in patent: Page/Page column 302
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