Identification | Back Directory | [Name]
2-Chloro-5-iodopyrimidine | [CAS]
32779-38-7 | [Synonyms]
2-Cloro-5-Iodopyrimidine Pyrimidine,2-chloro-5-iodo- 2-Chloro-5-iodopyrimidine,95% 2-Chloro-5-iodopyrimidine ISO 9001:2015 REACH | [Molecular Formula]
C4H2ClIN2 | [MDL Number]
MFCD06200210 | [MOL File]
32779-38-7.mol | [Molecular Weight]
240.43 |
Chemical Properties | Back Directory | [Melting point ]
133.0 to 137.0 °C | [Boiling point ]
318℃ | [density ]
2.187 | [Fp ]
146℃ | [storage temp. ]
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C | [form ]
powder to crystal | [pka]
-2.78±0.22(Predicted) | [color ]
White to Gray to Brown | [Sensitive ]
Light Sensitive | [InChI]
InChI=1S/C4H2ClIN2/c5-4-7-1-3(6)2-8-4/h1-2H | [InChIKey]
WSZRCNZXKKTLQE-UHFFFAOYSA-N | [SMILES]
C1(Cl)=NC=C(I)C=N1 |
Questions And Answer | Back Directory | [Description]
2-Chloro-5-iodopyrimidine is 2-Chloro-5-iodopyridine is a halo-substituted pyridine, and it is used in biology application as synthesis intermediate in the multi-step synthesis.
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Hazard Information | Back Directory | [Synthesis]
Step A. Preparation of 2-chloro-5-iodopyrimidine
To a stirred solution of 5-iodopyrimidin-2-amine (2.21 g, 10.0 mmol) in acetonitrile (20 mL) was sequentially added copper(II) chloride (2.02 g, 15 mmol) and tert-butyl nitrite (1.55 g, 15 mmol) at room temperature and under argon protection. The reaction mixture was transferred to an oil bath preheated to 60 °C and reacted under argon atmosphere. After completion of the reaction, the mixture was cooled to room temperature and diluted with the addition of ether (20 mL). The insoluble material was removed by filtration and the filtrate was concentrated under reduced pressure. The crude product was dissolved in a small amount of dichloromethane (about 2 mL) and purified by passing through an 80 g ISCO silica gel column using a 20 min gradient elution (0% to 100% ethyl acetate/hexane). 2-Chloro-5-iodopyrimidine (778 mg, 31% yield) was finally obtained as an off-white solid.1H NMR (400 MHz, CDCl3) δ 8.79 (s, 2H). | [References]
[1] Journal of Organic Chemistry, 2008, vol. 73, # 23, p. 9326 - 9333 [2] Patent: WO2010/9183, 2010, A1. Location in patent: Page/Page column 79 [3] Patent: US4248618, 1981, A [4] Patent: WO2013/186692, 2013, A1. Location in patent: Page/Page column 62 |
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