5-iodopyrimidin-4-amine
5-iodopyrimidin-4-amine Basic information
- Product Name:
- 5-iodopyrimidin-4-amine
- Synonyms:
-
- 5-iodopyrimidin-4-amine
- 4-Amino-5-iodopyrimidine
- 5-Iodo-pyrimidin-4-ylamine
- 4-Pyrimidinamine,5-iodo-
- 5-iodopyrimidin-4-amine ISO 9001:2015 REACH
- CAS:
- 91416-96-5
- MF:
- C4H4IN3
- MW:
- 221
- Product Categories:
-
- pyrimidine
- Heterocycle-Pyrimidine series
- Mol File:
- 91416-96-5.mol
5-iodopyrimidin-4-amine Chemical Properties
- Melting point:
- 188-189 °C
- Boiling point:
- 322.7±27.0 °C(Predicted)
- Density
- 2.204±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
- pka
- 3.86±0.10(Predicted)
- Appearance
- Light yellow to green yellow Solid
- InChI
- InChI=1S/C4H4IN3/c5-3-1-7-2-8-4(3)6/h1-2H,(H2,6,7,8)
- InChIKey
- HTBFTDHEWCRQPJ-UHFFFAOYSA-N
- SMILES
- C1=NC=C(I)C(N)=N1
5-iodopyrimidin-4-amine Usage And Synthesis
Synthesis
163133-86-6
91416-96-5
The general procedure for the synthesis of 4-amino-5-iodopyrimidine from the compound (CAS:163133-86-6) is as follows: 4-aminopyridine (0.970 g, 10.3 mmol) was dissolved in 20 mL of acetic acid, and iodine monochloride (1.67 g, 10.3 mmol, 1.01 eq.) was added to produce a large amount of N-iodine-substituted intermediates precipitate immediately in the reaction system. The reaction mixture was refluxed for 3 hours under argon protection. Upon completion of the reaction, the mixture was cooled to about 10 °C with a water bath to induce complete precipitation of the product. The precipitate was collected by filtration and dried to give 4-amino-5-iodopyrimidine as a pale yellow solid (1.4 g, 62% yield).
References
[1] Heterocycles, 1984, vol. 22, # 5, p. 1195 - 1210
[2] Synthesis (Germany), 2012, vol. 44, # 22, p. 3496 - 3504
[3] Patent: WO2005/30213, 2005, A1. Location in patent: Page/Page column 177
[4] Journal of the Society of Chemical Industry, London, 1950, vol. 69, p. 353
[5] Patent: US6541505, 2003, B1
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5-iodopyrimidin-4-amine(91416-96-5)Related Product Information
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- 4,5-Diaminopyrimidine
- 4-Amino-6-methoxypyrimidine
- 5-BROMOPYRIMIDIN-4-AMINE
- 5-Bromo-2-hydroxypyrimidine
- 4-AMINO-6-CHLOROPYRIMIDIN-5-YLAMINE
- 5-iodopyrimidin-4-amine
- 5-IODO-6-METHYL-4-PYRIMIDINAMINE
- 4-HYDRAZINO-5-IODO-2,6-DIMETHYLPYRIMIDINE
- 4-AMINO-5-IODO-6-HYDROXYPYRIMIDINE
- 4-AMINO-2-CHLORO-5-IODOPYRIMIDINE
- 5-IODO-N-(3-METHOXYPROPYL)-2,6-DIMETHYL-4-PYRIMIDINAMINE
- 4-(3,5-DIMETHYL-1H-PYRAZOL-1-YL)-5-IODO-2,6-DIMETHYLPYRIMIDINE
- 5-IODO-2,6-DIMETHYL-4-PYRIMIDINYLAMINE
- 4-AMINO-5-IODO-2-PYRIMIDINOL
- N-CYCLOHEXYL-5-IODO-2,6-DIMETHYL-4-PYRIMIDINAMINE
- 4-(5-IODO-2,6-DIMETHYL-4-PYRIMIDINYL)MORPHOLINE
- N'-(5-IODO-2,6-DIMETHYL-4-PYRIMIDINYL)-2,2-DIMETHYLPROPANOHYDRAZIDE