2-PYRIDINAMINE, 4-CHLORO-5-IODO-

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Products Intro: Product Name:2-Amino-4-chloro-5-iodopyridine
CAS:670253-37-9
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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CAS:670253-37-9
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CAS:670253-37-9
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Products Intro: Product Name:4-chloro-5-iodopyridin-2-amine
CAS:670253-37-9
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Products Intro: Product Name:4-chloro-5-iodopyridin-2-amine
CAS:670253-37-9
Purity:95% Package:100g; 1kg Remarks:LN00171088

2-PYRIDINAMINE, 4-CHLORO-5-IODO- manufacturers

2-PYRIDINAMINE, 4-CHLORO-5-IODO- Basic information
Product Name:2-PYRIDINAMINE, 4-CHLORO-5-IODO-
Synonyms:2-PYRIDINAMINE, 4-CHLORO-5-IODO-;2-Amino-4-chloro-5-iodopyridine;4-Chloro-5-iodo-2-pyridinamine;4-Chloro-5-iodo-pyridin-2-ylaMine;2-Amino-4-chloro-5-iodopyridine 98%
CAS:670253-37-9
MF:C5H4ClIN2
MW:254.46
EINECS:
Product Categories:
Mol File:670253-37-9.mol
2-PYRIDINAMINE, 4-CHLORO-5-IODO- Structure
2-PYRIDINAMINE, 4-CHLORO-5-IODO- Chemical Properties
Boiling point 326.8±42.0 °C(Predicted)
density 2.139±0.06 g/cm3 (20 ºC 760 Torr)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka3.87±0.24(Predicted)
AppearanceWhite to off-white Solid
InChIInChI=1S/C5H4ClIN2/c6-3-1-5(8)9-2-4(3)7/h1-2H,(H2,8,9)
InChIKeyMBEBQNFNTISDFJ-UHFFFAOYSA-N
SMILESC1(N)=NC=C(I)C(Cl)=C1
Safety Information
Hazard Codes Xn
Risk Statements 22-37/38-41
Safety Statements 26-39
HS Code 2933399990
MSDS Information
2-PYRIDINAMINE, 4-CHLORO-5-IODO- Usage And Synthesis
Synthesis
2-Amino-4-chloropyridine

19798-80-2

2-PYRIDINAMINE, 4-CHLORO-5-IODO-

670253-37-9

General procedure for the synthesis of 4-chloro-5-iodo-2-aminopyridine from 2-amino-4-chloropyridine: 2-amino-4-chloropyridine (1.00 g, 7.78 mmol) was dissolved in N,N-dimethylformamide (DMF, 40 mL), and the reaction flask was covered with aluminum foil to avoid light. N-iodosuccinimide (NIS, 970 mg, 4.28 mmol) was subsequently added. The reaction mixture was stirred at room temperature for 19 hours, then NIS (970 mg, 4.28 mmol) was added again and stirring was continued for 24 hours. Upon completion of the reaction, the reaction was quenched by the addition of deionized water (200 mL) and extracted with ethyl acetate (EtOAc, 2 x 250 mL). The organic phases were combined, washed sequentially with deionized water (2 × 200 mL) and saturated saline (200 mL), dried over anhydrous sodium sulfate (Na2SO4), and concentrated under reduced pressure. The crude product was recrystallized with ethanol (EtOH), and the mother liquor was recrystallized again to obtain orange needle-like crystals of the target product 4-chloro-5-iodo-2-aminopyridine (1.45 g, 73% yield).

References[1] European Journal of Medicinal Chemistry, 2014, vol. 84, p. 404 - 416
[2] Patent: WO2015/100609, 2015, A1. Location in patent: Page/Page column 47
[3] Patent: US2012/245144, 2012, A1. Location in patent: Page/Page column 125-126
[4] Journal of Medicinal Chemistry, 2016, vol. 59, # 3, p. 985 - 1002
[5] Patent: WO2013/91011, 2013, A1. Location in patent: Page/Page column 64
2-PYRIDINAMINE, 4-CHLORO-5-IODO- Preparation Products And Raw materials
Raw materials2-Amino-4-chloropyridine-->N-Iodosuccinimide-->N,N-Dimethylformamide
Tag:2-PYRIDINAMINE, 4-CHLORO-5-IODO-(670253-37-9) Related Product Information
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