4-Iodo-5-methylpyridin-2-amine
- Product Name
- 4-Iodo-5-methylpyridin-2-amine
- CAS No.
- 1227581-81-8
- Chemical Name
- 4-Iodo-5-methylpyridin-2-amine
- Synonyms
- 4-Iodo-5-methylpyridin-2-amine;4-Iodo-5-methyl-2-pyridinamine;2-Amino-4-Iodo-5-Methylpyridine;2-Pyridinamine, 4-iodo-5-methyl-;4-Iodo-5-methyl-pyridin-2-ylamine
- CBNumber
- CB43042140
- Molecular Formula
- C6H7IN2
- Formula Weight
- 234.04
- MOL File
- 1227581-81-8.mol
4-Iodo-5-methylpyridin-2-amine Property
- Boiling point:
- 316.0±42.0 °C(Predicted)
- Density
- 1.898±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- pka
- 6.20±0.24(Predicted)
- Appearance
- Off-white to light yellow Solid
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- I737325
- Product name
- 4-Iodo-5-methylpyridin-2-amine
- Packaging
- 10mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- AK148253
- Product name
- 4-Iodo-5-methylpyridin-2-amine
- Purity
- 97%
- Packaging
- 100mg
- Price
- $129
- Updated
- 2021/12/16
- Product number
- A431394
- Product name
- 4-Iodo-5-methylpyridin-2-amine
- Purity
- 97%
- Packaging
- 250mg
- Price
- $176
- Updated
- 2021/12/16
- Product number
- A431394
- Product name
- 4-Iodo-5-methylpyridin-2-amine
- Purity
- 97%
- Packaging
- 1g
- Price
- $352
- Updated
- 2021/12/16
- Product number
- CM174390
- Product name
- 4-iodo-5-methylpyridin-2-amine
- Purity
- 97%
- Packaging
- 1g
- Price
- $449
- Updated
- 2021/12/16
4-Iodo-5-methylpyridin-2-amine Chemical Properties,Usage,Production
Synthesis
153034-94-7
1227581-81-8
The general procedure for the synthesis of 4-iodo-5-methylpyridin-2-amine from 2-fluoro-4-iodo-5-methylpyridine was as follows: 2-fluoro-4-iodo-5-methylpyridine (3.00 g, 12.7 mmol) was mixed with concentrated aqueous ammonium hydroxide (3.5 mL, 90 mmol) in DMSO (17 mL) to form a white suspension. The reaction mixture was placed in a microwave reactor and reacted at 140 °C for 4 hours. After the reaction was completed, it was cooled to room temperature. The reaction mixture was diluted with EtOAc and water to separate the organic and aqueous layers. The aqueous layer was extracted with EtOAc (3 x 50 mL), all organic layers were combined and concentrated under reduced pressure. The concentrated residue was adsorbed onto silica gel and purified by fast silica gel chromatography with an elution gradient of 0 to 10% MeOH in DCM solution, resulting in 4-iodo-5-methylpyridin-2-amine (800 mg, 27% yield) as a white solid. The product was confirmed by 1H NMR (300 MHz, DMSO-d6, 27 °C): δ 2.13 (s, 3H), 5.81 (s, 2H), 6.99 (s, 1H), 7.75 (s, 1H). Mass spectral analysis showed m/z: ES+ [M+H]+ 235.
References
[1] Patent: US2016/376287, 2016, A1. Location in patent: Paragraph 0957
[2] Patent: WO2011/26904, 2011, A1. Location in patent: Page/Page column 131
[3] Patent: WO2012/87519, 2012, A1. Location in patent: Page/Page column 122
4-Iodo-5-methylpyridin-2-amine Preparation Products And Raw materials
Raw materials
Preparation Products
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