6-CHLORO-4-AMINO-2-METHOXYPYRIMIDINE
6-CHLORO-4-AMINO-2-METHOXYPYRIMIDINE Basic information
- Product Name:
- 6-CHLORO-4-AMINO-2-METHOXYPYRIMIDINE
- Synonyms:
-
- 6-CHLORO-4-AMINO-2-METHOXYPYRIMIDINE
- 4-Amino-6-chloro-2-methoxypyrimidine
- 4-Pyrimidinamine, 6-chloro-2-methoxy-
- 6-CHLORO-4-AMINO-2-METHOXYPYRIMIDINE ISO 9001:2015 REACH
- CAS:
- 3286-55-3
- MF:
- C5H6ClN3O
- MW:
- 159.57
- Product Categories:
-
- Heterocycle-Pyrimidine series
- Mol File:
- 3286-55-3.mol
6-CHLORO-4-AMINO-2-METHOXYPYRIMIDINE Chemical Properties
- Melting point:
- 128-129 °C(Solv: benzene (71-43-2))
- Boiling point:
- 337.8±45.0 °C(Predicted)
- Density
- 1.398±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- form
- solid
- pka
- 1.70±0.10(Predicted)
- color
- Pale yellow
6-CHLORO-4-AMINO-2-METHOXYPYRIMIDINE Usage And Synthesis
Synthesis
10132-07-7
124-41-4
3286-55-3
General procedure for the synthesis of 4-amino-6-chloro-2-methoxypyrimidine from 4-amino-2,6-dichloropyrimidine and sodium methanol: Sodium methanol (12 mL, 25% wt of methanol solution) was added to methanol (300 mL), followed by addition of 4-amino-2,6-dichloropyrimidine (5.00 g, 30.5 mmol) to the mixture. The reaction mixture was heated to reflux for 2 h. After completion of the reaction, the solution was evaporated to dryness. The residue was treated with deionized water (250 mL) and the precipitate formed was separated by filtration and dried under vacuum to afford the title product 4-amino-6-chloro-2-methoxypyrimidine as a white solid (3 g, 61% yield). The structure of the product was confirmed by 1H NMR (400 MHz, CDCl3): δ 3.92 (3H, s), 5.21 (2H, br s), 6.14 (1H, s).
References
[1] Patent: WO2005/47279, 2005, A1. Location in patent: Page/Page column 34
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