4-Amino-6-chloro-5-methoxypyrimidine
4-Amino-6-chloro-5-methoxypyrimidine Basic information
- Product Name:
- 4-Amino-6-chloro-5-methoxypyrimidine
- Synonyms:
-
- 6-CHLORO-5-METHOXYPYRIMIDIN-4-AMINE
- 4-AMINO-6-CHLORO-5-METHOXYPYRIMIDINE
- 4-Amino-6-Chloro-5-Methoxy Pyrimidin
- 6-Chloro-5-methoxy-4-pyrimidinamine
- 6-Chloro-5-MethoxypyriMidin-4-ylaMine
- 4-(p-AMinobenzene SulfonaMino)-5Methoxy-6-Chloro PyriMidine)
- 4-Pyrimidinamine, 6-chloro-5-methoxy-
- 4-Amino-6-chloro-5-methoxypyrimidine ISO 9001:2015 REACH
- CAS:
- 5018-41-7
- MF:
- C5H6ClN3O
- MW:
- 159.57
- EINECS:
- 225-700-5
- Product Categories:
-
- Halogenated Heterocycles ,Imidazoles
- Heterocycle-Pyrimidine series
- Pyrimidine
- Mol File:
- 5018-41-7.mol
4-Amino-6-chloro-5-methoxypyrimidine Chemical Properties
- Melting point:
- 176-178 °C
- Boiling point:
- 305.4±37.0 °C(Predicted)
- Density
- 1.398±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- pka
- 1.51±0.10(Predicted)
- Appearance
- White to off-white Solid
- InChI
- InChI=1S/C5H6ClN3O/c1-10-3-4(6)8-2-9-5(3)7/h2H,1H3,(H2,7,8,9)
- InChIKey
- AAJZJNHQPBMCFV-UHFFFAOYSA-N
- SMILES
- C1=NC(Cl)=C(OC)C(N)=N1
- CAS DataBase Reference
- 5018-41-7(CAS DataBase Reference)
4-Amino-6-chloro-5-methoxypyrimidine Usage And Synthesis
Synthesis
5018-38-2
5018-41-7
General procedure for the synthesis of 4-sulfo-5-methoxy-6-chloropyrimidine from 4,6-dichloro-5-methoxypyrimidine: a mixture of 4,6-dichloro-5-methoxypyrimidine (5.0 g, 28.1 mmol), 30% ammonia (45 mL), and n-butanol (15 mL) was heated and reacted in a sealed tube for 8 hr at 85 °C. Upon completion of the reaction, the reaction mixture was concentrated under reduced pressure and the concentrate was subsequently suspended in brine (150 mL). A white precipitate was collected by filtration and the filter cake was recrystallized from ethanol to afford the target compound 4-sulfo-5-methoxy-6-chloropyrimidine as an off-white solid in a yield of 4.1 g in 90% yield. The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 7.97 (s, 1H), 7.29 (s, 2H), 3.71 (s, 3H). Mass spectrum (ESI, cation mode) showed m/z: 159.91 [M + H]+.
References
[1] European Journal of Medicinal Chemistry, 2018, vol. 143, p. 1148 - 1164
[2] Patent: CN108164548, 2018, A. Location in patent: Paragraph 0209; 0210; 0211
[3] Organic Process Research and Development, 2015, vol. 19, # 6, p. 639 - 645
[4] Patent: WO2005/47279, 2005, A1. Location in patent: Page/Page column 33
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