ChemicalBook > Product Catalog >Pharmaceutical intermediates >Heterocyclic compound >Pyrimidines >Aminopyrimidine >2-Pyrimidinamine, N-methyl- (9CI)

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

2-Pyrimidinamine, N-methyl- (9CI) Suppliers list
Company Name: Fuyang JSK Biomedical Technology Co., Ltd  Gold
Tel: 18915409046
Email: 1102409417@qq.com
Company Name: Wuhan Chemwish Technology Co., Ltd  
Tel: 86-027-67849912
Email: sales@chemwish.com
Company Name: JinYan Chemicals(ShangHai) Co.,Ltd.  
Tel: 13817811078
Email: sales@jingyan-chemical.com
Company Name: Shanghai Hanhong Scientific Co.,Ltd.  
Tel: 021-54306202 13764082696
Email: info@hanhongsci.com
Company Name: Shandong Xiya Chemical Co., Ltd  
Tel: 13355009207 13355009207
Email: 3007715519@qq.com

2-Pyrimidinamine, N-methyl- (9CI) manufacturers

2-Pyrimidinamine, N-methyl- (9CI) Basic information
Product Name:2-Pyrimidinamine, N-methyl- (9CI)
Synonyms:2-Pyrimidinamine, N-methyl- (9CI);N-Methyl-2-pyrimidinamine;methyl(pyrimidin-2-yl)amine;NSC 102272;2-PyriMidinaMine, N-Methyl-;2-Pyrimidinamine, N-methyl- (9CI) ISO 9001:2015 REACH
CAS:931-61-3
MF:C5H7N3
MW:109.13
EINECS:
Product Categories:PYRIMIDINE
Mol File:931-61-3.mol
2-Pyrimidinamine, N-methyl- (9CI) Structure
2-Pyrimidinamine, N-methyl- (9CI) Chemical Properties
Melting point 60-62℃
Boiling point 216℃
density 1.144
Fp 85℃
storage temp. 2-8°C(protect from light)
form Solid
pka3.90±0.10(Predicted)
AppearanceWhite to yellow Solid
InChIInChI=1S/C5H7N3/c1-6-5-7-3-2-4-8-5/h2-4H,1H3,(H,6,7,8)
InChIKeyBQNXHDSGGRTFNX-UHFFFAOYSA-N
SMILESC1(NC)=NC=CC=N1
Safety Information
HS Code 2933599590
MSDS Information
2-Pyrimidinamine, N-methyl- (9CI) Usage And Synthesis
Synthesis
2-Chloropyrimidine

1722-12-9

Methylamine

74-89-5

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

931-61-3

Step 1: Synthesis of N-methylpyrimidin-2-amine To a solution of 2-chloropyrimidine (1 g, 8.7 mmol) in methanol (10 mL) was slowly added a methanolic solution of 2Methylamine (13.2 mL, 26.2 mmol) followed by potassium carbonate (2.5 g, 18 mmol). The reaction flask was sealed and the reaction was stirred at 80 °C overnight. Upon completion of the reaction, the mixture was cooled to room temperature and concentrated by rotary evaporator to remove volatile solvents. The residue was extracted by liquid-liquid partition with distilled water and dichloromethane. The organic layer was separated, dried over anhydrous sodium sulfate, filtered and concentrated to give 2-methylaminopyrimidine (290 mg, 30% yield) as a brown oil.

References[1] Bulletin of the Chemical Society of Japan, 1998, vol. 71, # 8, p. 1973 - 1991
[2] Journal of Medicinal Chemistry, 2013, vol. 56, # 17, p. 6626 - 6637
[3] Molecules, 2004, vol. 9, # 7, p. 520 - 526
[4] Patent: WO2011/71716, 2011, A1. Location in patent: Page/Page column 99
[5] Journal of the American Chemical Society, 1954, vol. 76, p. 1065,1067
2-Pyrimidinamine, N-methyl- (9CI) Preparation Products And Raw materials
Raw materials2-Chloropyrimidine-->Methylamine-->Potassium carbonate-->Methanol
Preparation Products5-Bromo-2-(methylamino)pyrimidine
Tag:2-Pyrimidinamine, N-methyl- (9CI)(931-61-3) Related Product Information
Pirimiphos ethyl ETHIRIMOL Dipyridamole 2-Cyanoamino-4,6-dihydroxypyrimidine Pirimicarb Pipemidic acid 2-(1-Piperazinyl)pyrimidine Pirimiphos-methyl BUPIRIMATE 2-Phenylaminoadenosine N-[(4-methoxyphenyl)methyl]pyrimidin-2-amine 2-CYANIMINO-4-METHYLPYRIMIDINE 2-ACETOACETAMINOPYRIMIDINE 2-DIMETHYLAMINO-6-HYDROXYPURINE N-(4-Methylquinazolin-2-yl)guanidine 2-Cyanoamino-4-hydroxy-6-methylpyrimidine 4-AMINO-2-CYANIMINO-6-HYDROXYPYRIMIDINE 2-(1H-BENZIMIDAZOL-2-YLAMINO)-6-METHYL-4-PYRIMIDINOL