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165807-05-6

165807-05-6 Structure

165807-05-6 Structure
IdentificationBack Directory
[Name]

4-DIMETHOXYMETHYLPYRIMIDIN-2-YLAMINE
[CAS]

165807-05-6
[Synonyms]

4-(DIMETHOXYMETHYL)-2-PYRIMIDINAMINE
4-DIMETHOXYMETHYLPYRIMIDIN-2-YLAMINE
4-(Dimethoxymethyl)pyrimidin-2-amine
2-Amino-4-(dimethoxymethyl)pyrimidine
2-Pyrimidinamine, 4-(dimethoxymethyl)-
4-DIMETHOXYMETHYLPYRIMIDIN-2-YLAMINE, 95+%
4-(dimethoxymethyl)-1,2-dihydropyrimidin-2-imine
4-DIMETHOXYMETHYLPYRIMIDIN-2-YLAMINE ISO 9001:2015 REACH
[Molecular Formula]

C7H11N3O2
[MDL Number]

MFCD05864792
[MOL File]

165807-05-6.mol
[Molecular Weight]

169.18
Chemical PropertiesBack Directory
[Boiling point ]

295.3±48.0 °C(Predicted)
[density ]

1.200±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[form ]

solid
[pka]

3.34±0.10(Predicted)
[color ]

Off-white
[InChI]

InChI=1S/C7H11N3O2/c1-11-6(12-2)5-3-4-9-7(8)10-5/h3-4,6H,1-2H3,(H2,8,9,10)
[InChIKey]

OQINWXZQCAIVNK-UHFFFAOYSA-N
[SMILES]

C1(N)=NC=CC(C(OC)OC)=N1
Questions And AnswerBack Directory
[Uses]

4-Dimethoxymethylpyrimidin-2-ylamine is a useful research chemical.
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
Spectrum DetailBack Directory
[Spectrum Detail]

4-DIMETHOXYMETHYLPYRIMIDIN-2-YLAMINE(165807-05-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methylglyoxal 1,1-dimethyl acetal

6342-56-9

Guanidine hydrochloride

50-01-1

N,N-Dimethylformamide dimethyl acetal

4637-24-5

4-DIMETHOXYMETHYLPYRIMIDIN-2-YLAMINE

165807-05-6

1. Acetone aldehyde dimethyl acetal (10 g, 84 mmol) and N,N-dimethylformamide dimethyl acetal (10 g, 84 mmol) were dissolved in DMF (30 ml) in a round-bottomed flask and the reaction was heated for 15 h at 110 °C. 2. an aqueous solution of guanidine hydrochloride (12 g, 127 mmol) and NaOH (6.7 g, 169 mmol) was added to the reaction mixture. 3. The mixture was refluxed for 36 hours. 4. After completion of the reaction, the reaction material was cooled and filtered. 5. The product was purified by recrystallization from hot ethyl acetate to afford 2-amino-4-dimethoxymethylpyrimidine (10 g, 70% yield) as a white crystalline solid.

[References]

[1] Tetrahedron Letters, 2013, vol. 54, # 28, p. 3715 - 3717
[2] Patent: EP1227092, 2002, A2. Location in patent: Page 25
[3] Patent: EP1229035, 2002, A1. Location in patent: Page 25
[4] Patent: EP1227091, 2002, A2. Location in patent: Page 25
[5] Patent: WO2007/104053, 2007, A2. Location in patent: Page/Page column 36-37
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