ChemicalBook--->CAS DataBase List--->105763-77-7

105763-77-7

105763-77-7 Structure

105763-77-7 Structure
IdentificationBack Directory
[Name]

2,4-Dichloro-6-methoxyquinazoline
[CAS]

105763-77-7
[Synonyms]

2,4-Dichloro-6-methoxyqui...
2,4-Dichloro-6-methoxyquinazoline
6-Methoxy-2,4-dichloroquinazoline
Quinazoline,2,4-dichloro-6-methoxy-
[Molecular Formula]

C9H6Cl2N2O
[MDL Number]

MFCD09954880
[MOL File]

105763-77-7.mol
[Molecular Weight]

229.06
Chemical PropertiesBack Directory
[Melting point ]

171 °C
[Boiling point ]

315.9±24.0 °C(Predicted)
[density ]

1.450
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

-0.67±0.30(Predicted)
[Appearance]

Off-white to light yellow Solid
[InChI]

InChI=1S/C9H6Cl2N2O/c1-14-5-2-3-7-6(4-5)8(10)13-9(11)12-7/h2-4H,1H3
[InChIKey]

WEAMQTSRMCCGSJ-UHFFFAOYSA-N
[SMILES]

N1=C2C(C=C(OC)C=C2)=C(Cl)N=C1Cl
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[Hazard Codes ]

T
[Risk Statements ]

25
[Safety Statements ]

45
[RIDADR ]

UN2811
[HazardClass ]

IRRITANT
Spectrum DetailBack Directory
[Spectrum Detail]

2,4-Dichloro-6-methoxyquinazoline(105763-77-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

6-METHOXYQUINAZOLINE-2,4-DIOL

32618-84-1

2,4-Dichloro-6-methoxyquinazoline

105763-77-7

Method F1: Synthesis of 2,4-dichloro-6-methoxyquinazoline (xa) To a mixture of 6-methoxyquinazoline-2,4(1H,3H)-dione (9.63 g, 50.2 mmol) and phosphorus trichloride (POCl3, 150 mL) was added N,N-dimethylaniline (0.5 mL). The reaction mixture was stirred at 120 °C for 2 hours. Upon completion of the reaction, the excess POCl3 was removed by distillation under reduced pressure. the residue was slowly poured into ice water and the pH was adjusted to about 7 by slowly adding saturated sodium bicarbonate (NaHCO3) solution at 0 °C, where a precipitate was formed. The precipitate was collected and dried under vacuum to give 2,4-dichloro-6-methoxyquinazoline (11.2 g, 98% yield) as a brown solid. LCMS m/z = 229.1, 231.0 [M + 1] (Method B) (retention time = 1.87 min). 1H-NMR (400 MHz, DMSO-d6): δ 7.89 (d, J = 9.2 Hz, 1H), 7.71 (dd, J = 8.8, 2.4 Hz, 1H), 7.38 (d, J = 1.6 Hz, 1H), 3.91 (s, 3H).

[References]

[1] Patent: US2015/307477, 2015, A1. Location in patent: Paragraph 1497
[2] Patent: JP6121658, 2017, B2. Location in patent: Paragraph 1096; 1099
[3] Patent: US2010/68197, 2010, A1. Location in patent: Page/Page column 17
[4] Bioorganic and Medicinal Chemistry, 2003, vol. 11, # 11, p. 2439 - 2444
[5] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 24, p. 7717 - 7727
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