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CAS No. : | 252932-48-2 | MDL No. : | MFCD06797655 |
Formula : | C7H10N2O2 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | SPNDLEQTZLQLTA-UHFFFAOYSA-N |
M.W : | 154.17 | Pubchem ID : | 2773439 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P280-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302-H315-H319-H332-H335 | Packing Group: | N/A |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
81% | With sodium cyanoborohydride;acetic acid; In methanol; at 20 - 50℃; | A reaction mixture of 3-amino-lH-pyrrole-2-carboxylic acid ethyl ester (0.77 g, 4.99 mmol), lH-benzoimidazole-2-carboxaldehyde (0.88 g, 5.99 mmol), NaCNBH3 (0.31 g, 4.99 mmol) and HOAc (0.57 mL, 9.99 mmol) in methanol (15 mL) was stirred at r.t. overnight. The mixture was then heated at 50 °C for 5 h. Cooled to r.t. and evaporated in vacuo. The residue was dissolved in ethyl acetate and washed with water. The aqueous phase was extracted with ethyl acetate (twice). The combined organic layers were dried (MgSO4) and concentrated. The crude product was purified by flash column chromatography (heptane/ethyl acetate (1:0 to 0:1), obtaining 1.15 g (81percent) of the title compound. 1H NMR (DMSO-d6) delta ppm 12.27 (IH, s), 10.85 (IH, s), 7.63 - 7.37 (2H, m), 7.17 - 7.08 (2H, m), 6.71 (IH, t, J=3.0 Hz), 5.99 (IH, br s), 5.60 (IH, t, J=2.7 Hz), 4.48 (2H, d, J=5.8 Hz), 4.22 (2H, q, J=7.1 Hz), 1.29 (3H, t, J=7.1 Hz); EPO <DP n="56"/>MS (ESI) m/z 285 (M +1). |
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