4-Pyrimidinamine, 6-chloro-5-methyl- (9CI)
4-Pyrimidinamine, 6-chloro-5-methyl- (9CI) Basic information
- Product Name:
- 4-Pyrimidinamine, 6-chloro-5-methyl- (9CI)
- Synonyms:
-
- 4-Pyrimidinamine, 6-Chloro-5-Methyl
- 6-AMINO-4-CHLORO-5-METHYLPYRIMIDINE
- 4-Amino-6-chloro-5-methylpyrimidine
- 6-Chloro-5-methyl-pyrimidin-4-ylamine
- 4-Pyrimidinamine, 6-chloro-5-methyl- (9CI)
- 6-chloro-5-methylpyrimidin-4-amine
- 6-Chloro-5-methyl-4-pyrimidinamine
- 4-Pyrimidinamine, 6-chloro-5-methyl- (9CI) ISO 9001:2015 REACH
- CAS:
- 14394-56-0
- MF:
- C5H6ClN3
- MW:
- 143.57
- Product Categories:
-
- Heterocycle-Pyrimidine series
- PYRIMIDINE
- Mol File:
- 14394-56-0.mol
4-Pyrimidinamine, 6-chloro-5-methyl- (9CI) Chemical Properties
- Melting point:
- 237-238℃
- Boiling point:
- 292.4±35.0 °C(Predicted)
- Density
- 1.349±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- pka
- 2.41±0.10(Predicted)
- Appearance
- White to off-white Solid
4-Pyrimidinamine, 6-chloro-5-methyl- (9CI) Usage And Synthesis
Synthesis
4316-97-6
14394-56-0
4,6-Dichloro-5-methylpyrimidine (Sigma-Aldrich No. 595446, 5 g, 30.70 mmol) was used as starting material and dissolved in a methanol solution of 7 M ammonia (15 ml, 105 mmol). The reaction mixture was placed in a sealed vial and the reaction was stirred at 140 °C for 40 min. After completion of the reaction, the resulting white suspension was poured into a mixture of water (300 ml) and ethyl acetate (600 ml), shaken well and left to stratify. The aqueous phase was separated and extracted with ethyl acetate (3 x 600 ml). The organic phases were combined, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford the target compound 6-chloro-5-methyl-4-pyrimidinamine (3.10 g, 20.73 mmol, 68% yield) as a white solid. The product was analyzed by UPLC (retention time: 0.41 min) and the mass spectrum showed major peaks at m/z 144 ([M+H]+, 100%) and m/z 146 ([M+H]+, 33%), which was in accordance with the theoretical molecular weight of 143 (C5H6ClN3).1H NMR (400 MHz, DMSO-d6) δ (ppm): 8.06 (s, 1H) , 7.09 (bs, 2H), 2.07 (s, 3H).
References
[1] Patent: WO2009/3997, 2009, A1. Location in patent: Page/Page column 18
[2] Journal of the Chemical Society, 1947, p. 41,45
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4-Pyrimidinamine, 6-chloro-5-methyl- (9CI)(14394-56-0)Related Product Information
- 4-AMINO-6-CHLORO-PYRIMIDINE-5-CARBALDEHYDE
- 4-Pyrimidinamine, 6-chloro-2-methyl- (9CI)
- 2-Pyrimidinamine, 4-chloro-6-methyl- (9CI)
- 4-Pyrimidinamine, 2-chloro-5-methyl- (9CI)
- 2-Pyrimidinamine, 4-chloro-N-methyl- (9CI)
- Pyrimidine, 4-amino-5-chloro-6-methyl- (7CI,8CI)
- 4-Pyrimidinamine, 2-chloro-6-methyl- (9CI)
- 4-Pyrimidinamine, 6-chloro-N-methyl- (9CI)
- 4-CHLORO-6-MORPHOLINO-5-PYRIMIDINECARBALDEHYDE
- 6-Chloro-2,5-dimethyl-4-pyrimidinamine
- 2-Pyrimidinamine, 4-chloro-5-methyl- (9CI)
- 2-Pyrimidinamine, 5-chloro-4-methyl- (9CI)
- 5-Pyrimidinamine, 4-chloro-2-methyl- (9CI)
- 4-Pyrimidinamine, 2-chloro-N-methyl- (9CI)
- 5-Pyrimidinamine, 2-chloro-4-methyl- (9CI)
- 2-Pyrimidinamine, 5-chloro-N-methyl- (9CI)
- 4-Pyrimidinamine, 5-chloro-2-methyl- (9CI)
- 2-CHLORO-6-METHYLPYRIMIDIN-4-AMINE