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ChemicalBook--->CAS DataBase List--->5018-41-7

5018-41-7

5018-41-7 Structure

5018-41-7 Structure
IdentificationMore
[Name]

4-Amino-6-chloro-5-methoxypyrimidine
[CAS]

5018-41-7
[Synonyms]

4-AMINO-6-CHLORO-5-METHOXYPYRIMIDINE
6-CHLORO-5-METHOXYPYRIMIDIN-4-AMINE
4-Amino-6-Chloro-5-Methoxy Pyrimidin
6-Chloro-5-methoxy-4-pyrimidinamine
[EINECS(EC#)]

225-700-5
[Molecular Formula]

C5H6ClN3O
[MDL Number]

MFCD07787635
[Molecular Weight]

159.57
[MOL File]

5018-41-7.mol
Chemical PropertiesBack Directory
[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)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H335-H319
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
[HS Code ]

2933599590
Spectrum DetailBack Directory
[Spectrum Detail]

4-Amino-6-chloro-5-methoxypyrimidine(5018-41-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

4,6-Dichloro-5-methoxypyrimidine

5018-38-2

4-Amino-6-chloro-5-methoxypyrimidine

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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