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6-chloro-Nmethylpyrimidin-4-amine

6-chloro-Nmethylpyrimidin-4-amine Suppliers list
Company Name: Beijing Bosennuokang Pharmaceutical Technology Co., Ltd.  Gold
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6-chloro-Nmethylpyrimidin-4-amine manufacturers

6-chloro-Nmethylpyrimidin-4-amine Basic information
Product Name:6-chloro-Nmethylpyrimidin-4-amine
Synonyms:6-chloro-Nmethylpyrimidin-4-amine;4-Pyrimidinamine, 6-chloro-N-methyl- (9CI);4-Chloro-6-methylaminopyrimidine;EOS-60926;4-Pyrimidinamine, 6-chloro-N-methyl-;6-chloro-Nmethylpyrimidin-4-amine ISO 9001:2015 REACH
CAS:65766-32-7
MF:C5H6ClN3
MW:143.57
EINECS:
Product Categories:amine|alkyl chloride;Amines;PYRIMIDINE;blocks;APIs & Intermediate
Mol File:65766-32-7.mol
6-chloro-Nmethylpyrimidin-4-amine Structure
6-chloro-Nmethylpyrimidin-4-amine Chemical Properties
Melting point 138-142°C
Boiling point 279.7±20.0 °C(Predicted)
density 1.338±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka2.50±0.10(Predicted)
form solid
AppearanceWhite to off-white Solid
InChIInChI=1S/C5H6ClN3/c1-7-5-2-4(6)8-3-9-5/h2-3H,1H3,(H,7,8,9)
InChIKeyWZVLJUBTIWFTIE-UHFFFAOYSA-N
SMILESC1=NC(Cl)=CC(NC)=N1
Safety Information
Hazard Codes Xn
Risk Statements 22-36/37/38-43
Safety Statements 26-36/37/39
WGK Germany 3
HazardClass IRRITANT
HS Code 2933599590
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
Skin Sens. 1
STOT SE 3
MSDS Information
6-chloro-Nmethylpyrimidin-4-amine Usage And Synthesis
Synthesis
4,6-Dichloropyrimidine

1193-21-1

Methylamine hydrochloride

593-51-1

6-chloro-Nmethylpyrimidin-4-amine

65766-32-7

General procedure for the synthesis of 6-chloro-N-methyl-4-aminopyrimidine from 4,6-dichloropyrimidine and methylamine hydrochloride: in a 100 mL round-bottomed flask N,N-dimethylformamide (10 mL), 4,6-dichloropyrimidine (1 g, 6.71 mmol, 1.0 equiv.), cesium carbonate (4.4 g, 13.50 mmol, 2.01 equiv.) and methylamine hydrochloride (905 mg, 13.40 mmol, 2.00 eq.). The reaction mixture was stirred at 80 °C for 14 hours. After completion of the reaction, the reaction solution was diluted with 10 mL of water and extracted with ethyl acetate (4 x 10 mL). The organic layers were combined and washed once with 10 mL of water. The organic phase was concentrated under reduced pressure and the resulting residue was purified by silica gel column chromatography with ethyl acetate/petroleum ether (1:1) as eluent. 750 mg (78% yield) of the target product 6-chloro-N-methyl-4-aminopyrimidine was finally obtained as a white solid. The product was analyzed by LC-MS to confirm: (ES, m/z): retention time RT = 0.476 min, LCMS 32: m/z = 144 [M + 1].

References[1] European Journal of Organic Chemistry, 2014, vol. 2014, # 7, p. 1514 - 1524
[2] Patent: WO2017/181177, 2017, A1. Location in patent: Paragraph 0950-0953
[3] Tetrahedron, 2007, vol. 63, # 25, p. 5394 - 5405
6-chloro-Nmethylpyrimidin-4-amine Preparation Products And Raw materials
Raw materials4,6-Dichloropyrimidine-->Methylamine-->Methylamine hydrochloride-->N,N-Dimethylformamide-->Cesium carbonate
Tag:6-chloro-Nmethylpyrimidin-4-amine(65766-32-7) Related Product Information
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