| Identification | More | [Name]
ETHYL 2-CHLOROOXAZOLE-4-CARBOXYLATE | [CAS]
460081-18-9 | [Synonyms]
2-CHLOROOXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER
ETHYL 2-CHLOROOXAZOLE-4-CARBOXYLATE
Ethyl 2-chloro-1,3-oxazole-4-carboxylate
4-Oxazolecarboxylicacid,2-chloro-,ethylester(9CI)
2-CHLOROOXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER, 95+% | [Molecular Formula]
C6H6ClNO3 | [MDL Number]
MFCD06660120 | [Molecular Weight]
175.57 | [MOL File]
460081-18-9.mol |
| Chemical Properties | Back Directory | [Melting point ]
97-98℃ | [Boiling point ]
254.1±32.0 °C(Predicted) | [density ]
1.332±0.06 g/cm3(Predicted) | [storage temp. ]
Keep Cold | [pka]
-3.20±0.10(Predicted) | [Appearance]
White to pink Solid | [InChI]
InChI=1S/C6H6ClNO3/c1-2-10-5(9)4-3-11-6(7)8-4/h3H,2H2,1H3 | [InChIKey]
SYWQOPRAPDMWMC-UHFFFAOYSA-N | [SMILES]
O1C=C(C(OCC)=O)N=C1Cl | [CAS DataBase Reference]
460081-18-9(CAS DataBase Reference) |
| Hazard Information | Back Directory | [Synthesis]
Under nitrogen protection, 1.70 mL (14.3 mmol) of tert-butyl nitrite was added dropwise to a suspension of 1.65 g (12.3 mmol) cuprous(I) chloride in 50 mL of acetonitrile. The reaction mixture was heated to 75 °C, followed by the addition of 1.60 g (10.2 mmol) of ethyl 2-aminooxazole-4-carboxylate in batches over 20 min (Ref: G Crank MJ Foulis, J Med Chem 1971,14:1075-1077). Gases were released during the reaction. After continued stirring for 30 min, the reaction mixture was cooled to room temperature, diluted with 50 mL of ethyl acetate and washed with water (2 x 25 mL). The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give a dark oily solid. Purification by neutral silica gel column chromatography using a solvent mixture of hexane and ethyl acetate (3:1) afforded 1.27 g (71% yield) of the target compound, ethyl 2-chloroxazole-4-carboxylate, as white needle-like crystals (recrystallized from hexane). Mass spectrum (electrospray positive ion mode): m/z 176/177 [M+H]+. 1H NMR (CDCl3) δ: 1.47 (t, 3H, J = 7.16 Hz); 4.48 (q, 2H, J = 7.16 Hz); 8.28 (s, 1H). | [References]
[1] Organic Letters, 2003, vol. 5, # 16, p. 2911 - 2914
[2] Organic Letters, 2002, vol. 4, # 17, p. 2905 - 2907
[3] European Journal of Medicinal Chemistry, 2019, p. 80 - 108
[4] Patent: WO2005/26149, 2005, A1. Location in patent: Page/Page column 111
[5] Journal of Medicinal Chemistry, 2010, vol. 53, # 9, p. 3814 - 3830 |
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