|
|
| | 5,7-dichlorothiazolo[5,4-d]pyrimidine Basic information |
| Product Name: | 5,7-dichlorothiazolo[5,4-d]pyrimidine | | Synonyms: | 5,7-dichloro-[1,3]thiazolo[5,4-d]pyriMidine;5,7-dichlorothiazolo[5,4-d]pyrimidine;Thiazolo[5,4-d]pyrimidine, 5,7-dichloro- | | CAS: | 13479-88-4 | | MF: | C5HCl2N3S | | MW: | 206.05 | | EINECS: | | | Product Categories: | Heterocycle-Pyrimidine series | | Mol File: | 13479-88-4.mol | ![5,7-dichlorothiazolo[5,4-d]pyrimidine Structure](CAS/GIF/13479-88-4.gif) |
| | 5,7-dichlorothiazolo[5,4-d]pyrimidine Chemical Properties |
| Melting point | 148.5-149.5 °C | | Boiling point | 281.2±22.0 °C(Predicted) | | density | 1.767±0.06 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | solubility | DMF: 2 mg/ml,DMSO: 1 mg/ml,Ethanol: insol,PBS (pH 7.2): insol | | form | A solid | | pka | -2.68±0.50(Predicted) | | color | Light yellow to brown | | InChI | InChI=1S/C5HCl2N3S/c6-3-2-4(11-1-8-2)10-5(7)9-3/h1H | | InChIKey | XYBGDWLYHQAUQM-UHFFFAOYSA-N | | SMILES | C1(Cl)=NC(Cl)=C2N=CSC2=N1 |
| | 5,7-dichlorothiazolo[5,4-d]pyrimidine Usage And Synthesis |
| Uses | 5,7-Dichlorothiazolo[5,4-d]pyrimidine was used in studies to prepare Kinase inhibitors. | | Synthesis | The general procedure for the synthesis of 5,7-dichlorothiazolo[5,4-d]pyrimidine using thiazolo[5,4-d]pyrimidine-5,7(4H,6H)-dione as starting material was as follows: a 10 mL round bottom flask was charged with intermediate 45.2 (100 mg, 0.59 mmol, 1.00 equiv.), N,N-diisopropylethylamine (DIEA, 0.5 mL) and phosphorus oxychloride (POCl3, 2 mL). The reaction mixture was stirred at 100 °C for 12 hours. After completion of the reaction, the mixture was concentrated under reduced pressure to remove the solvent. The crude product was purified by fast column chromatography to afford intermediate 45.3 (100 mg, 82% yield) as a yellow oil. | | References | [1] Heterocycles, 2012, vol. 85, # 7, p. 1721 - 1726
[2] Patent: WO2015/48281, 2015, A1. Location in patent: Paragraph 00472; 00475
[3] Patent: WO2014/15291, 2014, A1. Location in patent: Page/Page column 168; 169
[4] Journal of the American Chemical Society, 1951, vol. 73, p. 3862 |
| | 5,7-dichlorothiazolo[5,4-d]pyrimidine Preparation Products And Raw materials |
|