ChemicalBook--->CAS DataBase List--->42839-09-8

42839-09-8

42839-09-8 Structure

42839-09-8 Structure
IdentificationMore
[Name]

2-Pyrimidinemethanol
[CAS]

42839-09-8
[Synonyms]

2-(HYDROXYMETHYL)-PYRIMIDINE
2-PYRIMIDINEMETHANOL
PYRIMIDIN-2-YLMETHANOL
2-Pyrimidinemethanol (7CI,9CI)
(PYRIMIDIN-2-YL)METHANOL,PURITY:95% MIN(HPLC)
[Molecular Formula]

C5H6N2O
[MDL Number]

MFCD06796201
[Molecular Weight]

110.11
[MOL File]

42839-09-8.mol
Chemical PropertiesBack Directory
[Boiling point ]

198.2±23.0 °C(Predicted)
[density ]

1.227±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

DMF: 30 mg/ml; DMSO: 30 mg/ml; Ethanol: 100 mg/ml; PBS (pH 7.2): 10 mg/ml
[form ]

A crystalline solid
[pka]

13.61±0.10(Predicted)
[color ]

Colorless to light yellow
[CAS DataBase Reference]

42839-09-8(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Flame (GHS02)Corrosion (GHS05)Exclamation Mark (GHS07)
GHS02,GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H225-H302-H315-H318-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[RIDADR ]

1993
[HazardClass ]

3
[PackingGroup ]

Ⅲ
[HS Code ]

2933998090
Hazard InformationBack Directory
[Uses]

2-?Pyrimidinemethanol is a reactant used in the synthesis of avanafil, which is used to treat erectile dysfunction. Also used in the synthesis of
[Synthesis]

2-PYRIMIDINECARBOXYLIC ACID, METHYL ESTER

34253-03-7

2-Pyrimidinemethanol

42839-09-8

Synthesis of pyrimidin-2-ylmethanol (12): ester 11 (0.43 g, 3.09 mmol) was dissolved in EtOH (30 mL), stirred and cooled to 0 °C. NaBH4 (0.114 g, 3.09 mmol) was slowly added under stirring and the reaction mixture continued to stir for 2 hours. The progress of the reaction was monitored by thin layer chromatography (TLC) and after confirming complete consumption of the raw materials, the reaction was quenched with cold water. Subsequently, the reaction mixture was concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography with MeOH/CH2Cl2 (1:49) as eluent to afford alcohol 12 (0.145 g, 37% yield). The product had an Rf value of 0.3 in 10% MeOH/CHCl3.1H NMR (500 MHz, CDCl3) δ: 8.75 (d, J = 5.5 Hz, 2H), 7.26-7.22 (m, 1H), 4.85 (s, 2H). Mass spectrum (ESI): m/z 111.1 [M+H]+.

[References]

[1] Patent: WO2013/13238, 2013, A2. Location in patent: Page/Page column 33
[2] Patent: US2010/63066, 2010, A1. Location in patent: Page/Page column 15
[3] Patent: US2007/49603, 2007, A1. Location in patent: Page/Page column 53; 78
[4] Patent: WO2012/40230, 2012, A1. Location in patent: Page/Page column 80-81
[5] Patent: WO2013/142269, 2013, A1. Location in patent: Paragraph 0507; 0508
Spectrum DetailBack Directory
[Spectrum Detail]

2-Pyrimidinemethanol(42839-09-8)1HNMR
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