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ChemicalBook--->CAS DataBase List--->5439-14-5

5439-14-5

5439-14-5 Structure

5439-14-5 Structure
IdentificationBack Directory
[Name]

3,4-DIHYDRO-2H-PYRIDO[1,2-A]PYRIMIDIN-2-ONE
[CAS]

5439-14-5
[Synonyms]

ACID CAPTOR H
LABOTEST-BB LT00847264
Dihydropyridopyrimidinone
3,4-dihydropyrido[1,2-a]pyrimidin-2-one
3,4-DIHYDRO-2-PYRIDOL[1,2-A]PYRIMIDINONE
3,4-DIHYDRO-2H-PYRIDO[1,2-A]PYRIMIDIN-2-ONE
2H-Pyrido[1,2-a]pyrimidin-2-one,3,4-dihydro-
3,4-Dihydro-2H-pyrido[1,2-a]pyrimidin-2-one >
3,4-Dihydro-2iHi-pyrido[1,2-iai]pyrimidin-2-one
3,4-DIHYDRO-2H-PYRIDO[1,2-A]PYRIMIDIN-2-ONE 98+%
3,4-DIHYDRO-2H-PYRIDO[1,2-A]PYRIMIDIN-2-ONE ISO 9001:2015 REACH
[EINECS(EC#)]

226-618-2
[Molecular Formula]

C8H8N2O
[MDL Number]

MFCD00042798
[MOL File]

5439-14-5.mol
[Molecular Weight]

148.16
Chemical PropertiesBack Directory
[Melting point ]

185-187 °C
[Boiling point ]

271℃
[density ]

1.26
[Fp ]

118℃
[storage temp. ]

2-8°C
[solubility ]

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

Solid
[pka]

2.83±0.20(Predicted)
[color ]

Light Yellow
[BRN ]

3667723
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Safety Statements ]

22-24/25
[WGK Germany ]

3
[F ]

9-23
[HS Code ]

29339900
Hazard InformationBack Directory
[Preparation]

3,4-Dihydro-2h-pyrido[1,2-a]pyrimidin-2-one is prepared by reaction of 2-aminopyridine with either Acrylic Acid itself or an  equivalent (2-bromo- or 2-iodopropionic acid, Methyl Acrylate, ethyl 2-bromopropionate, β- Propiolactone).
[storage]

The reagent may be dried over P2O5 in vacuo (135 °C/17 mmHg).
[Purification Methods]

Dissolve it in CHCl3, filter, evaporate, then recrystallise the residue from EtOH/Me2CO (needles) which can be washed with Et2O and dried. It can also be recrystallised from CHCl3/pet ether or CHCl3/hexane. The hydrochloride has m 295-295o (dec, from EtOH or MeOH/Et2O), the hydrobromide has m 299-300o(dec) (from MeOH/Et2O) and the picrate has m 224-226o(corr), m 219-220o from EtOH. [Adams & Pachter J Am Chem Soc 74 4906 1952, Lappin J Org Chem 23 1358 1958, Hurd & Hayao J Am Chem Soc 77 115 1955, Beilstein 24 III/IV 299.]
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