2,4-Dichloro-6,7-dimethoxyquinazoline
2,4-Dichloro-6,7-dimethoxyquinazoline Basic information
- Product Name:
- 2,4-Dichloro-6,7-dimethoxyquinazoline
- Synonyms:
-
- TIMTEC-BB SBB000972
- 2,4-DICHLORO-6,7-DIMETHOXYQUINAZOLINE
- 2,4-Dichloro-6,7-dimethoxyquin
- Doxazosin Impurity 5(Doxazosin EP Impurity E)
- Doxazosin Impurity 6
- 2-Chloro-6,7-diMethoxyquinazolin-4-yl Chloride
- 2,4-Dichloro-6-Methoxy-7-quinazolinyl Methyl ether
- Doxazosin Related Compound E (20 mg) (2,4-dichloro-6,7-dimethoxyquinazoline)
- CAS:
- 27631-29-4
- MF:
- C10H8Cl2N2O2
- MW:
- 259.09
- EINECS:
- 608-117-4
- Product Categories:
-
- Building Blocks
- Halogenated Heterocycles
- Heterocyclic Building Blocks
- Quinazolines
- QuinazolinesHeterocyclic Building Blocks
- Aromatics
- Heterocycles
- Intermediates & Fine Chemicals
- Pharmaceuticals
- Quinoline&Isoquinoline
- Quinolines, Quinazolines and derivatives
- Heterocycles series
- Mol File:
- 27631-29-4.mol
2,4-Dichloro-6,7-dimethoxyquinazoline Chemical Properties
- Melting point:
- 175-178 °C (lit.)
- Boiling point:
- 340.5±42.0 °C(Predicted)
- Density
- 1.5369 (rough estimate)
- refractive index
- 1.6100 (estimate)
- storage temp.
- 2-8°C
- solubility
- Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
- pka
- -0.49±0.30(Predicted)
- form
- Crystalline Powder
- color
- Pale yellow to beige
- Water Solubility
- Insoluble in water.
- Sensitive
- Moisture Sensitive
- BRN
- 190331
- CAS DataBase Reference
- 27631-29-4(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 37/39-26-36
- WGK Germany
- 3
- HS Code
- 29334900
2,4-Dichloro-6,7-dimethoxyquinazoline Usage And Synthesis
Chemical Properties
pale yellow to beige crystalline powder
Uses
An intermediate in the preparation of potential inhibitors of epidermal growth factor receptor kinases. An intermediate in the preparation of Terazosin (T105000).
Uses
2,4-Dichloro-6,7-dimethoxyquinazoline is used as an intermediate in the preparation of potential inhibitors of epidermal growth factor receptor kinases. It is also used as an intermediate in the preparation of terazosin.
Synthesis
28888-44-0
27631-29-4
The general procedure for the synthesis of 2,4-dichloro-6,7-dimethoxyquinazoline from 6,7-dimethoxy-2,4-quinazolinedione was as follows: in a 100 mL three-necked flask equipped with a reflux condenser, 6,7-dimethoxy-2,4-quinazolinedione (1.00 g) and phosphorus triclosan (15 mL; 24.77 g; 161.53 mmol) were added, the reaction mixture was refluxed at 100 °C in an oil bath with stirring for 24 hours. Upon completion of the reaction, the reaction solution was cooled to room temperature and the reaction was quenched by slowly pouring it into an ice-water mixture under vigorous stirring. The precipitated solid was collected by vacuum filtration and the crude product was purified by silica gel column chromatography using dichloromethane as eluent.
References
[1] Journal of Medicinal Chemistry, 1986, vol. 29, # 5, p. 627 - 629
[2] European Journal of Medicinal Chemistry, 2014, vol. 71, p. 1 - 14
[3] Patent: WO2004/13091, 2004, A2. Location in patent: Page 34-35
[4] The Journal of organic chemistry, 2002, vol. 67, # 23, p. 8284 - 8286
[5] Journal of the Chemical Society, 1948, p. 1759,1765
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2,4-Dichloro-6,7-dimethoxyquinazoline(27631-29-4)Related Product Information
- Dimethyl carbonate
- Quinazoline
- Metformin
- Primaquine diphosphate
- Dimethyldimethoxysilane
- Sulfaquinoxaline
- 2-Chloropyrimidine
- 2-Chloroquinazoline
- 2-CHLORO-6,7-DIMETHOXYQUINAZOLINE
- 4-CHLORO-6-HYDROXYQUINAZOLINE
- 4-CHLORO-QUINAZOLINE
- 4-Chloro-7-methoxyquinazoline
- 2,4-Dichloroquinazoline
- 2,4-Dichloro-7-methoxyquinazoline
- 2,4-Dichloro-6-methoxyquinazoline
- 2,4-Dichloropyrimidine
- 4-Chloro-6,7-dimethoxyquinazoline
- 4-CHLORO-7-HYDROXYQUINAZOLINE