2-CHLORO-4-PHENYLQUINAZOLINE
2-CHLORO-4-PHENYLQUINAZOLINE Basic information
- Product Name:
- 2-CHLORO-4-PHENYLQUINAZOLINE
- Synonyms:
-
- 2-CHLORO-4-PHENYLQUIZOLINE
- Quinazoline,2-chloro-4-phenyl-
- 2-CHLORO-4-PHENYLQUINAZOLIN
- oro-4-phenyL
- quinazoL
- 2-CHLORO-4-PHENYLQUINAZOLINE ISO 9001:2015 REACH
- 2-CHLORO-4-PHENYLQUINAZOLINE
- 2-Chloro-4-phenylq inazollne
- CAS:
- 29874-83-7
- MF:
- C14H9ClN2
- MW:
- 240.69
- EINECS:
- 201-615-9
- Product Categories:
-
- quinazoline
- Mol File:
- 29874-83-7.mol
2-CHLORO-4-PHENYLQUINAZOLINE Chemical Properties
- Melting point:
- 113.0 to 117.0 °C
- Boiling point:
- 347.4±30.0 °C(Predicted)
- Density
- 1.285±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- powder to crystal
- pka
- 0.24±0.30(Predicted)
- color
- White to Orange to Green
- InChI
- InChI=1S/C14H9ClN2/c15-14-16-12-9-5-4-8-11(12)13(17-14)10-6-2-1-3-7-10/h1-9H
- InChIKey
- SFKMVPQJJGJCMI-UHFFFAOYSA-N
- SMILES
- N1=C2C(C=CC=C2)=C(C2=CC=CC=C2)N=C1Cl
2-CHLORO-4-PHENYLQUINAZOLINE Usage And Synthesis
Uses
2-Chloro-4-phenylquinazoline acts as a reagent in the synthesis of MTH1 inhibitors that are potential cancer eradicators.
Uses
2-Chloro-4-phenylquinazoline acts as a reagent in the synthesis of MTH1 inhibitors that are potential cancer eradicators.
Uses
2-CHLORO-4-PHENYLQUINAZOLINE can be used as organic synthesis intermediate and pharmaceutical intermediate, mainly used in laboratory research and development process and chemical production process.
Synthesis
A 2 L flask was charged with 35.0 g (175.8 mmol) of 2,4-dichloroquinoline,22.5 g (184.6 mmol) of phenylboronic acid, 6.1 g (5.3 mmol) of tetrakis(triphenylphosphine)palladium(0) were added to 800 mL of tetrahydrofuran and 400 mL of water, and the mixture was heated to 60 ?? C for 12 hours under a nitrogen stream. . The resulting mixture was added to methanol (3000 mL), and the crystallized solid was filtered and dissolved in toluene, filtered through silica gel / celite, and the organic solvent was removed in an appropriate amount, and then recrystallization from methanol gave Intermediate I-A52-1 (36.8 g, 87% yield).
References
[1] Patent: KR2017/10582, 2017, A. Location in patent: Paragraph 0251-0254
[2] Patent: KR2016/74426, 2016, A. Location in patent: Paragraph 0162; 0163; 0164; 0165
[3] Patent: KR2017/97450, 2017, A. Location in patent: Paragraph 0317-0319; 0337-0339
[4] Patent: WO2012/67425, 2012, A1. Location in patent: Page/Page column 39-40
[5] Patent: WO2012/36482, 2012, A1. Location in patent: Page/Page column 27-28
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