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4-Amino-2-(methylthio)pyrimidine-5-carbaldehyde

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CAS:770-31-0
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CAS:770-31-0
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Products Intro: Product Name:4-Amino-2-(methylthio)pyrimidine-5-carbaldehyde
CAS:770-31-0
Purity:>=98% Package:0.25g;1g;5g;10g;25g;100g;500g

4-Amino-2-(methylthio)pyrimidine-5-carbaldehyde manufacturers

4-Amino-2-(methylthio)pyrimidine-5-carbaldehyde Basic information
Product Name:4-Amino-2-(methylthio)pyrimidine-5-carbaldehyde
Synonyms:4-AMINO-2-METHYLTHIO-PYRIMIDINE-5-CARBALDEHYDE;4-aMino-2-Methanesulfanyl-pyriMidine-5-carboxaldehyde;4-AMino-2-(Methylthio)-5-pyriMidinecarboxaldehyde;4-Amino-2-(methylthio)pyrimidine-5-carboxaldehyde;2-METHYLTHIO 4-AMINO 5-FORMYL PYRIMIDINE;5-PYRIMIDINECARBOXALDEHYDE, 4-AMINO-2-(METHYLTHIO)-;4-Amino-2-(methylthio)pyrimidine-5-carbaldehyde ISO 9001:2015 REACH;Benzene,1-ethenyl-8-nitro-
CAS:770-31-0
MF:C6H7N3OS
MW:169.2
EINECS:220-644-8
Product Categories:Amines;Aromatics;Heterocycles;Sulfur & Selenium Compounds
Mol File:770-31-0.mol
4-Amino-2-(methylthio)pyrimidine-5-carbaldehyde Structure
4-Amino-2-(methylthio)pyrimidine-5-carbaldehyde Chemical Properties
Melting point 183-184 °C
Boiling point 379.7±27.0 °C(Predicted)
density 1.37
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
form solid
pka2.50±0.10(Predicted)
color White
InChIInChI=1S/C6H7N3OS/c1-11-6-8-2-4(3-10)5(7)9-6/h2-3H,1H3,(H2,7,8,9)
InChIKeyFGONQMFYFJRAIG-UHFFFAOYSA-N
SMILESC1(SC)=NC=C(C=O)C(N)=N1
Safety Information
HS Code 2933599590
MSDS Information
4-Amino-2-(methylthio)pyrimidine-5-carbaldehyde Usage And Synthesis
Uses4-Amino-2-(methylthio)pyrimidine-5-carbaldehyde can be used for the preparation of pyridopyrimidines and naphthyridines as inhibitors of Akt kinase for the treatment of cancer.
Synthesis
(4-AMINO-2-(METHYLTHIO)PYRIMIDIN-5-YL)METHANOL

588-36-3

4-Amino-2-(methylthio)pyrimidine-5-carbaldehyde

770-31-0

Method A: Manganese dioxide (MnO2, 49.8 g, 572 mmol) was added to a chloroform (818 mL) suspension of 4-amino-2-(methylthio)pyrimidin-5-ylmethanol (28 g, 164 mmol), and the reaction mixture was stirred for 4 hours at 55°C (internal temperature). After completion of the reaction, the reaction mixture was filtered while hot and the filter cake was washed with hot chloroform and tetrahydrofuran (THF). The filtrates were combined, concentrated under reduced pressure and subsequently dried under vacuum to afford 4-amino-2-methylmercaptopyrimidine-5-carbaldehyde (26.7 g, 96% yield) as a light yellow solid. Mass spectrometry (MS) data: m/z 170.1 ([M+H]+).

References[1] Journal of Medicinal Chemistry, 2000, vol. 43, # 24, p. 4606 - 4616
[2] Patent: WO2013/134243, 2013, A1. Location in patent: Page/Page column 17
[3] Journal of Medicinal Chemistry, 2015, vol. 58, # 10, p. 4165 - 4179
[4] Patent: WO2014/182829, 2014, A1. Location in patent: Page/Page column 42
[5] Patent: WO2016/191172, 2016, A1. Location in patent: Page/Page column 57
Tag:4-Amino-2-(methylthio)pyrimidine-5-carbaldehyde(770-31-0) Related Product Information
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