ChemicalBook--->CAS DataBase List--->331647-05-3

331647-05-3

331647-05-3 Structure

331647-05-3 Structure
IdentificationBack Directory
[Name]

8-BROMO-2,4-DICHLOROQUINAZOLINE
[CAS]

331647-05-3
[Synonyms]

2,4-DICHLORO-8-BROMOQUINAZOLINE
8-BROMO-2,4-DICHLOROQUINAZOLINE
Quinazoline, 8-bromo-2,4-dichloro-
8-BROMO-2,4-DICHLOROQUINAZOLINE ISO 9001:2015 REACH
[Molecular Formula]

C8H3BrCl2N2
[MDL Number]

MFCD09954891
[MOL File]

331647-05-3.mol
[Molecular Weight]

277.936
Chemical PropertiesBack Directory
[Boiling point ]

330.2±24.0 °C(Predicted)
[density ]

1.851
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

-1.75±0.30(Predicted)
[Appearance]

Off-white to light yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P305+P351+P338-P337+P313-P261-P271-P304+P340-P312-P403+P233-P405-P501
[HazardClass ]

IRRITANT
[HS Code ]

2933599590
Questions And AnswerBack Directory
[Application]

8-Bromo-2,4-Dichloroquinazoline is a quinazoline derivative, which is mainly used as an intermediate in pharmaceutical and chemical synthesis.
Spectrum DetailBack Directory
[Spectrum Detail]

8-BROMO-2,4-DICHLOROQUINAZOLINE(331647-05-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

8-bromoquinazoline-2,4(1H,3H)-dione

331646-99-2

8-BROMO-2,4-DICHLOROQUINAZOLINE

331647-05-3

8-Bromoquinazoline-2,4(1H,3H)-dione (12.1 g, 50 mmol, 1 eq.) was used as starting material, which was dissolved in phosphorous trichloride (POCl3, 130 mL), followed by the addition of N,N-dimethylformamide (DMF, 0.5 mL) as catalyst. The reaction mixture was stirred at 130 °C for 12 h. After completion of the reaction, the reaction was cooled to room temperature. The reaction mixture was concentrated by rotary evaporator. The concentrated residue was dissolved in ethyl acetate (EA, 100 mL) and quenched by slowly pouring into ice water under vigorous stirring. The organic phase was separated, washed with saturated saline, dried over anhydrous sodium sulfate (Na2SO4), filtered and concentrated again. Finally, the target product 8-bromo-2,4-dichloroquinazoline was purified by column chromatography (eluent: petroleum ether/ethyl acetate = 10:1, v/v) as a yellow solid (9.1 g, 60% yield).

[References]

[1] Organic Letters, 2011, vol. 13, # 4, p. 676 - 679
[2] ACS Medicinal Chemistry Letters, 2018, vol. 9, # 9, p. 941 - 946
[3] Patent: WO2015/27222, 2015, A2. Location in patent: Paragraph 0214
[4] Patent: WO2016/133935, 2016, A1. Location in patent: Paragraph 0287
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