2-CHLORO-4-PHENYLPYRIMIDINE
2-CHLORO-4-PHENYLPYRIMIDINE Basic information
- Product Name:
- 2-CHLORO-4-PHENYLPYRIMIDINE
- Synonyms:
-
- 2-chloro-4-phenyl-pyrimidin
- 2-CHLORO-4-PHENYLPYRIMIDINE
- Pyrimidine, 2-chloro-4-phenyl-
- 2-Chloro-4-phenylpyrimidine95%
- 2-Chloro-6-phenylpyrimidine
- CAS:
- 13036-50-5
- MF:
- C10H7ClN2
- MW:
- 190.63
- Product Categories:
-
- Amines
- blocks
- APIs & Intermediate
- Pyrimidine
- pharmacetical
- Mol File:
- 13036-50-5.mol
2-CHLORO-4-PHENYLPYRIMIDINE Chemical Properties
- Melting point:
- 86 °C
- Boiling point:
- 368.3±11.0 °C(Predicted)
- Density
- 1.245±0.06 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,2-8°C
- pka
- -1.38±0.20(Predicted)
- Appearance
- White to off-white Solid
Safety Information
- Hazard Codes
- Xn
- Risk Statements
- 22-37/38-41
- Safety Statements
- 26-39
- HS Code
- 2933599590
2-CHLORO-4-PHENYLPYRIMIDINE Usage And Synthesis
Synthesis Reference(s)
The Journal of Organic Chemistry, 53, p. 4137, 1988 DOI: 10.1021/jo00252a057
Synthesis
3934-20-1
98-80-6
13036-50-5
General procedure for the synthesis of 2-chloro-4-phenylpyrimidines from 2,4-dichloropyrimidines and phenylboronic acid: first, 2,4-dichloropyrimidines (5 g, 33.57 mmol) were dissolved in acetonitrile (60 ml), followed by the addition of water (15 ml). Next, phenylboronic acid (4.09 g, 33.57 mmol) and sodium carbonate (14.23 g, 134.28 mmol) were added to this solution. Degassing was carried out by blowing nitrogen into the reaction mixture for 10 minutes. After that, tetrakis(triphenylphosphine)palladium (354 mg, 0.34 mmol) was added. The reaction mixture was stirred under nitrogen protection at 90 °C for 18 hours. After completion of the reaction, the mixture was filtered through diatomaceous earth and the filtrate was collected. The solvent was removed by distillation under reduced pressure and the crude product obtained was purified by column chromatography with the eluent being a 10-15% ethyl acetate/petroleum ether solvent mixture, resulting in the target compound 2-chloro-4-phenylpyrimidine as a colorless solid (2.98 g, 47% yield). Mass spectrum (LRMS) [M + H]+ m/z: 191.1; 1H NMR (400 MHz, CDCl3) δ 8.62 (d, J = 5.3 Hz, 1H), 8.16-7.99 (m, 2H), 7.63 (d, J = 5.3 Hz, 1H), 7.50 (qdd, J = 6.0,3.2,1.4 Hz, 3H).
References
[1] Journal of Organometallic Chemistry, 2018, vol. 862, p. 76 - 85
[2] Patent: CN103819455, 2016, B. Location in patent: Paragraph 0067; 0084; 0085
[3] Patent: KR2015/34146, 2015, A. Location in patent: Paragraph 0059; 0076; 0077
[4] Tetrahedron Letters, 2006, vol. 47, # 26, p. 4415 - 4418
[5] Patent: WO2011/93609, 2011, A1. Location in patent: Page/Page column 19
2-CHLORO-4-PHENYLPYRIMIDINE Preparation Products And Raw materials
Raw materials
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2-CHLORO-4-PHENYLPYRIMIDINE(13036-50-5)Related Product Information
- 2-CHLORO-4-PHENYLPYRIMIDINE
- Ethyl 2-chloro-4-phenylpyrimidine-5-carboxylate ,97%,ETHYL 2-CHLORO-4-PHENYLPYRIMIDINE-5-CARBOXYLATE
- 4-(3-Bromophenyl)-2-chloropyrimidine
- 2-AMINO-4-CHLORO-6-PHENYLPYRIMIDINE
- 2-CHLORO-4-PHENYLPYRIMIDINE-5-CARBONYL CHLORIDE
- 2-CHLORO-5-(4-METHOXYPHENYL)PYRIMIDINE
- 4-PHENYLIMIDAZOLE
- 2-CHLORO-6-METHYL-4-PHENYL-QUINAZOLINE
- 2,4-dichloro-6-phenylpyrimidine
- 2,6-DICHLORO-4-PHENYL-QUINAZOLINE
- 2-chloro-5-methyl-4-phenylpyrimidine
- 2-Chloro-4-(4-fluoro-phenyl)-pyrimidine
- 2-CHLORO-4-PHENYLQUINAZOLINE
- 6-BROMO-2-CHLORO-4-PHENYLQUINAZOLINE
- 2-Chloro-4,6-diphenylpyrimidine
- 4-CHLORO-6-PHENYLPYRIMIDINE
- 5-CHLORO-2-PHENYLPYRIMIDINE
- 6-AMINO-2-(4-BROMOPHENYL)-5-CHLOROPYRIMIDINE-4-CARBOXYLIC ACID