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2-Pyrimidinamine, 5-methyl- (9CI)

2-Pyrimidinamine, 5-methyl- (9CI) Suppliers list
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Products Intro: CAS:50840-23-8
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Products Intro: Product Name:5-Methylpyrimidin-2-amine
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Products Intro: Product Name:5-methylpyrimidin-2-amine
CAS:50840-23-8
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2-Pyrimidinamine, 5-methyl- (9CI) manufacturers

2-Pyrimidinamine, 5-methyl- (9CI) Basic information
Product Name:2-Pyrimidinamine, 5-methyl- (9CI)
Synonyms:2-Pyrimidinamine, 5-methyl- (9CI);5-methylpyrimidin-2-amine;2-amino-5-methylpyrimidine;5-Methyl-2-pyrimidinamine;5-Methylpyrimidine-2-amine;5-Methyl-2-aminopyrimidine;2-PyriMidinaMine, 5-Methyl-;5-Methyl-pyrimidin-2-ylamine
CAS:50840-23-8
MF:C5H7N3
MW:109.13
EINECS:
Product Categories:Heterocycle-Pyrimidine series;PYRIMIDINE
Mol File:50840-23-8.mol
2-Pyrimidinamine, 5-methyl- (9CI) Structure
2-Pyrimidinamine, 5-methyl- (9CI) Chemical Properties
Melting point 192-193℃
Boiling point 194.6°C (rough estimate)
density 1.155
refractive index 1.5340 (estimate)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka4.20±0.10(Predicted)
form solid
AppearanceWhite to yellow Solid
InChI1S/C5H7N3/c1-4-2-7-5(6)8-3-4/h2-3H,1H3,(H2,6,7,8)
InChIKeyMHZNCOBCMWBPPM-UHFFFAOYSA-N
SMILESCc1cnc(N)nc1
Safety Information
Hazard Codes Xn
Risk Statements 22
WGK Germany 3
HS Code 2933599590
Storage Class13 - Non Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
2-Pyrimidinamine, 5-methyl- (9CI) Usage And Synthesis
Uses5-Methylpyrimidin-2-amine is a useful research chemical compound used in the preparation of highly potent macrocyclic ALK inhibitors as potential antitumors.
Synthesis
2-Chloro-5-methylpyrimidine

22536-61-4

2-Pyrimidinamine, 5-methyl- (9CI)

50840-23-8

Step 1: 2-Chloro-5-methylpyrimidine (10.0 g, 77.79 mmol) was dissolved in industrial methanol (IMS, 100 mL) followed by addition of 35% ammonia (100 mL). The reaction mixture was transferred to an autoclave, sealed and reacted at 200 °C for 4 hours. Upon completion of the reaction, it was cooled to room temperature and most of the solvent was removed by concentration via rotary evaporator. Water (25 mL) was added to the residue and a solid was precipitated. The solid was collected by filtration and dried under vacuum to afford 2-amino-5-methylpyrimidine (7.85 g, 92% yield) as an off-white solid. The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 8.06 (s, 2H), 6.30 (s, 2H), 2.03 (s, 3H).LCMS analysis showed m/z 110 [M + H]+.

Purification MethodsCrystallise it from water or *benzene/pet ether and sublime it at 50o/0.5mm. [Beilstein 24 H 87.]
References[1] Patent: WO2013/132376, 2013, A1. Location in patent: Page/Page column 205
[2] Journal of Medicinal Chemistry, 2014, vol. 57, # 11, p. 4720 - 4744
[3] Chemische Berichte, 1905, vol. 38, p. 3397
[4] Bioorganic and Medicinal Chemistry Letters, 2017, vol. 27, # 5, p. 1261 - 1266
2-Pyrimidinamine, 5-methyl- (9CI) Preparation Products And Raw materials
Raw materials2-Chloro-5-methylpyrimidine-->2-[BIS(TERT-BUTOXYCARBONYL)AMINO]-5-BROMOPYRIMIDINE-->DIMETHYLZINC-->Water-->Ethanol-->Ammonia
Tag:2-Pyrimidinamine, 5-methyl- (9CI)(50840-23-8) Related Product Information
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