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2-Chloro-4-(4-fluoro-phenyl)-pyrimidine

Product Name
2-Chloro-4-(4-fluoro-phenyl)-pyrimidine
CAS No.
85979-59-5
Chemical Name
2-Chloro-4-(4-fluoro-phenyl)-pyrimidine
Synonyms
2-Chloro-4-(4-fluoro-phenyl);2-Chloro-4-(4-fluoro-phenyl)-pyrimidine;Pyrimidine, 2-chloro-4-(4-fluorophenyl)-
CBNumber
CB51079206
Molecular Formula
C10H6ClFN2
Formula Weight
208.62
MOL File
85979-59-5.mol
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2-Chloro-4-(4-fluoro-phenyl)-pyrimidine Property

Melting point:
125-126 °C
Boiling point:
364.2±17.0 °C(Predicted)
Density 
1.326±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Store in freezer, under -20°C
pka
-1.73±0.31(Predicted)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

AK Scientific
Product number
3406AC
Product name
2-Chloro-4-(4-fluoro-phenyl)-pyrimidine
Packaging
1g
Price
$477
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0128166
Product name
2-CHLORO-4-(4-FLUORO-PHENYL)-PYRIMIDINE
Purity
95.00%
Packaging
5MG
Price
$504.31
Updated
2021/12/16
Matrix Scientific
Product number
126333
Product name
2-Chloro-4-(4-fluoro-phenyl)-pyrimidine
Purity
>95%
Packaging
1g
Price
$810
Updated
2021/12/16
Chemenu
Product number
CM124050
Product name
2-chloro-4-(4-fluorophenyl)pyrimidine
Purity
95+%
Packaging
5g
Price
$948
Updated
2021/12/16
Crysdot
Product number
CD11042979
Product name
2-Chloro-4-(4-fluoro-phenyl)-pyrimidine
Purity
97%
Packaging
5g
Price
$1003
Updated
2021/12/16
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2-Chloro-4-(4-fluoro-phenyl)-pyrimidine Chemical Properties,Usage,Production

Synthesis

3934-20-1

1765-93-1

85979-59-5

To a stirred solution of 2,4-dichloropyrimidine (3.00 g, 20.1 mmol) in toluene (25 mL) were sequentially added 4-fluorophenylboronic acid (2.82 g, 20.1 mmol), potassium carbonate (8.32 g, 60.3 mmol), tetrakis(triphenylphosphine)palladium(0) (0.630 g, 0.545 mmol), and a 1:1 (v/v) ethanol/water solvent mixture (36 mL). The reaction mixture was heated and stirred at 55 °C for 12 h and subsequently concentrated under reduced pressure. The residue was diluted with water and extracted with ethyl acetate. The organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography using hexane/ethyl acetate as eluent to afford 2-chloro-4-(4-fluorophenyl)pyrimidine as a yellow solid (2.50 g, 61% yield). The above product (1.27 g, 6.09 mmol) was dissolved in N,N-dimethylformamide (8 mL) and ethyl piperidine-4-carboxylate (0.959 g, 6.10 mmol) and cesium carbonate (2.10 g, 6.44 mmol) were added. The reaction mixture was heated and stirred at 100 °C for 12 h and subsequently concentrated under reduced pressure. The residue was diluted with water and extracted with ethyl acetate. The organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography using hexane/ethyl acetate as eluent to afford ethyl 1-(4'-fluoro-[1,1'-biphenyl]-3-yl)piperidine-4-carboxylate as a yellow oil (1.60 g, 80% yield). The above intermediate (1.60 g, 4.80 mmol) was dissolved in a 1:1 (v/v) methanol/water solvent mixture (20 mL) and solid sodium hydroxide (0.968 g, 24.2 mmol) was added. The reaction was concentrated under reduced pressure after 2 hours. The residue was dissolved in water and the pH was adjusted to about 6 with 1N hydrochloric acid and subsequently extracted with ethyl acetate. The organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford 1-(4'-fluoro-[1,1'-biphenyl]-3-yl)piperidine-4-carboxylic acid as a white solid (1.40 g, 97% yield). Using General Method D, the above carboxylic acid was subjected to an amide coupling reaction with Intermediate 5, resulting in 2-chloro-4-(4-fluorophenyl)-pyrimidine as a white solid (0.118 g, 27% yield). 1H NMR (500 MHz, CDCl3) δ 8.37 (d, J = 5.0 Hz, 1H), 8.07-8.04 (m, 2H), 7.15 (t, J = 9.0 Hz, 2H), 6.89 (d, J = 10.0 Hz, 1H), 5.38 (s, 1H), 4.97-4.95 (m, 2H), 3.02-2.83 (m, 8H), 2.39-2.37 (m, 2H), 1.96-1.51 (m, 13H) ppm. 13C NMR (100 MHz, CDCl3) δ 174.1, 165.3, 163.3, 163.2, 161.7, 158.4, 133.8, 129.0, 128.9, 115.7, 115.5, 105.2, 59.4, 53.1, 47.6, 46.1, 44.6, 43.5, 39.3, 36.1, 28.9, 39.3, 36.1, 28.9, 39.3 36.1, 28.9, 28.7, 25.1, 24.3, 24.2 ppm. Purity: >96% (214 and 254 nm) LCMS; retention time: 1.44 min; (M+H+) 438.3.

References

[1] Patent: WO2014/43068, 2014, A1. Location in patent: Page/Page column 188; 189
[2] Synthesis, 2010, # 16, p. 2721 - 2724

2-Chloro-4-(4-fluoro-phenyl)-pyrimidine Preparation Products And Raw materials

Raw materials

Preparation Products

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2-Chloro-4-(4-fluoro-phenyl)-pyrimidine Suppliers

Shanghai Raise Chemical Technology Co.,Ltd
Tel
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0556-5030632
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China
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55
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Hangzhou Milestone Pharmtech Co., Ltd.
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Amadis Chemical Company Limited
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0086-571-89925065
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China
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Sichuan BaiPeng Biotechnology Co., Ltd.
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Aikon International Limited
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025-66061636 18013972705
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Shanghai ZiHao Pharmaceutical Co., Ltd.
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China
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Shanghai Jizhi Biochemical Technology Co. Ltd.
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China
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Shanghai Sealing Biotechnology Co. Ltd..
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China
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View Lastest Price from 2-Chloro-4-(4-fluoro-phenyl)-pyrimidine manufacturers

Career Henan Chemical Co
Product
2-Chloro-4-(4-fluoro-phenyl)-pyrimidine 85979-59-5
Price
US $1.00/KG
Min. Order
1KG
Purity
95%
Supply Ability
200KG
Release date
2018-08-19