ChemicalBook--->CAS DataBase List--->1353553-07-7

1353553-07-7

1353553-07-7 Structure

1353553-07-7 Structure
IdentificationBack Directory
[Name]

Thieno[3,2-d]pyrimidine, 2-chloro-4-(3-nitrophenoxy)-
[CAS]

1353553-07-7
[Synonyms]

2-chloro-4-(3-nitrophenoxy)thieno[3,2-d]pyrimidine
Thieno[3,2-d]pyrimidine, 2-chloro-4-(3-nitrophenoxy)-
[Molecular Formula]

C12H6ClN3O3S
[MDL Number]

MFCD30185158
[MOL File]

1353553-07-7.mol
[Molecular Weight]

307.71
Chemical PropertiesBack Directory
[storage temp. ]

Inert atmosphere,2-8°C
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

Thieno[3,2-d]pyrimidine, 2-chloro-4-(3-nitrophenoxy)-(1353553-07-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

2,4-Dichlorothieno[3,2-d]pyrimidine

16234-14-3

3-Nitrophenol

554-84-7

Thieno[3,2-d]pyrimidine, 2-chloro-4-(3-nitrophenoxy)-

1353553-07-7

Procedure for the synthesis of 2-chloro-4-(3-nitrophenoxy)thieno[3,2-d]pyrimidine: 2,4-dichlorothieno[3,2-d]pyrimidine (2.9 g, 14.2 mmol) was dissolved in N,N-dimethylformamide (70 mL), followed by the addition of 3-nitrophenol (1.9 g, 14.2 mmol) and cesium carbonate (9.2 g, 28.4 mmol ). The reaction mixture was stirred at room temperature for 1 hour. After completion of the reaction, distilled water was added to the mixture and the precipitate was collected by filtration under reduced pressure. The precipitate was washed with distilled water and dried under reduced pressure to afford the target compound 2-chloro-4-(3-nitrophenoxy)thieno[3,2-d]pyrimidine (4.0 g, 91.8% yield). The product was characterized by 1H-NMR (300 MHz, CDCl3): δ 8.25-8.17 (m, 2H), 8.08 (s, 1H), 7.69-7.66 (m, 2H), 7.57 (d, 1H).

[References]

[1] Patent: WO2011/162515, 2011, A2. Location in patent: Page/Page column 34-35
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