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4-(Methylamino)-2-(methylthio)pyrimidine-5-methanol

CAS No.
17759-30-7
Chemical Name:
4-(Methylamino)-2-(methylthio)pyrimidine-5-methanol
Synonyms
(4-MethylaMino-2-MethanethiopyriMidin-5-yl)Methanol;4-(MethylaMino)-2-(Methylthio)-5-pyriMidineMethanol;4-(Methylamino)-2-(methylthio)pyrimidine-5-methanol;5-Pyrimidinemethanol, 4-(methylamino)-2-(methylthio)-;(4-MethylaMino-2-MethylsulfanylpyriMidin-5-yl)Methanol;(4-(MethylaMino)-2-(Methylthio )pyriMidin-5-yl)Methanol;(4-MethylaMino-2-Methanesulfanyl-pyriMidin-5-yl)-Methanol
CBNumber:
CB32510337
Molecular Formula:
C7H11N3OS
Molecular Weight:
185.25
MDL Number:
MFCD16293863
MOL File:
17759-30-7.mol
MSDS File:
SDS
Last updated:2026-05-28 01:06:02

4-(Methylamino)-2-(methylthio)pyrimidine-5-methanol Properties

Melting point 155-157 °C
Boiling point 398.9±32.0 °C(Predicted)
Density 1.28±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
solubility Chloroform, Dichloromethane, DMSO, Methanol
form Solid
pka 13.16±0.10(Predicted)
color White

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338

4-(Methylamino)-2-(methylthio)pyrimidine-5-methanol price More Price(23)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC TRC-M286900-50MG 4-(Methylamino)-2-(methylthio)pyrimidine-5-methanol 50mg $129 2026-06-03 Buy
TRC TRC-M286900-250MG 4-(Methylamino)-2-(methylthio)pyrimidine-5-methanol 250mg $320 2026-06-03 Buy
TRC TRC-M286900-100MG 4-(Methylamino)-2-(methylthio)pyrimidine-5-methanol 100mg $217 2026-06-03 Buy
Usbiological 016502 4-(Methylamino)-2-(methylthio)pyrimidine-5-methanol 17759-30-7 100mg $531 2026-06-03 Buy
Matrix Scientific 126652 (4-(Methylamino)-2-(methylthio)-pyrimidin-5-yl)methanol 17759-30-7 1.00g $1044 2026-05-18 Buy
Product number Packaging Price Buy
TRC-M286900-50MG 50mg $129 Buy
TRC-M286900-250MG 250mg $320 Buy
TRC-M286900-100MG 100mg $217 Buy
016502 100mg $531 Buy
126652 1.00g $1044 Buy

4-(Methylamino)-2-(methylthio)pyrimidine-5-methanol Chemical Properties, Uses, Production

Chemical Properties

White Solid

Uses

An intermediate in the preparation of antitumor agents and tyrosine kinase inhibitors

Synthesis

ETHYL 4-(METHYLAMINO)-2-(METHYLSULFANYL)-5-PYRIMIDINECARBOXYLATE

76360-82-2

4-(Methylamino)-2-(methylthio)pyrimidine-5-methanol

17759-30-7

The general procedure for the synthesis of (4-methylamino-2-methanesulfonyl-pyrimidin-5-yl)-methanol from ethyl 4-methylamino-2-methylthio-5-pyrimidinecarboxylate was as follows: lithium aluminium hydride (11.48 g, 302 mmol) was suspended in 600 mL of anhydrous tetrahydrofuran (THF) in a 2 L three-necked flask fitted with an overhead stirrer, protected by argon gas. Another 250 mL round-bottomed flask was taken and ethyl 4-methylamino-2-methylthio-5-pyrimidine carboxylate (43.71 g, 0.192 mol) was dissolved in 200 mL of anhydrous THF and transferred through a cannula to a 250 mL addition funnel. The pyrimidine solution was slowly added dropwise to the lithium aluminum hydride suspension at room temperature for a controlled time of 30 minutes. After the dropwise addition was completed, the reaction was continued with stirring for 1 hour. Subsequently, 25 mL of water was carefully added dropwise over 30 minutes to quench the reaction. Next, 25 mL of 15% (w/v) aqueous sodium hydroxide solution and 75 mL of water were added sequentially, at which point the reaction mixture faded from a light green color and formed a light green slurry, and stirring was continued for 1 hour. Upon completion of the reaction, the precipitated aluminum salt was removed by vacuum filtration and the solid was washed well with ethyl acetate (EtOAc). The filtrate was concentrated to give a light yellow slurry. The slurry was suspended in 250 mL of a 25% EtOAc/hexane solvent mixture and the colorless solid was separated by vacuum filtration. After vacuum drying, 31.9 g (90% yield) of the target product (4-methylamino-2-methylthio-pyrimidin-5-yl)-methanol was obtained, and the spectral data were consistent with those reported in the literature.

References

[1] Patent: WO2004/63195, 2004, A1. Location in patent: Page 53-54
[2] Patent: WO2006/71940, 2006, A2. Location in patent: Page/Page column 355
[3] Patent: WO2008/33999, 2008, A2. Location in patent: Page/Page column 88
[4] Journal of Medicinal Chemistry, 2011, vol. 54, # 7, p. 2255 - 2265
[5] Patent: US2003/207900, 2003, A1. Location in patent: Page/Page column 15

4-(Methylamino)-2-(methylthio)pyrimidine-5-methanol Preparation Products And Raw materials

4-(Methylamino)-2-(methylthio)pyrimidine-5-methanol Suppliers

Global Suppliers ( 53)
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J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
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4-(Methylamino)-2-(methylthio)pyrimidine-5-methanol Spectrum

4-(Methylamino)-2-(methylthio)pyrimidine-5-methanol (4-(MethylaMino)-2-(Methylthio )pyriMidin-5-yl)Methanol (4-MethylaMino-2-MethanethiopyriMidin-5-yl)Methanol (4-MethylaMino-2-MethylsulfanylpyriMidin-5-yl)Methanol 4-(MethylaMino)-2-(Methylthio)-5-pyriMidineMethanol (4-MethylaMino-2-Methanesulfanyl-pyriMidin-5-yl)-Methanol 5-Pyrimidinemethanol, 4-(methylamino)-2-(methylthio)- 17759-30-7 Amines Aromatics Heterocycles Intermediates & Fine Chemicals Pharmaceuticals Sulfur & Selenium Compounds