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4-Amino-6-chloro-5-methoxypyrimidine

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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
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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)
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Safety Information

HS Code 
2933599590
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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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