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Chemical Structure| 1215626-40-6 Chemical Structure| 1215626-40-6

Structure of 1215626-40-6

Chemical Structure| 1215626-40-6

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Product Details of [ 1215626-40-6 ]

CAS No. :1215626-40-6
Formula : C15H22N4O4
M.W : 322.36
SMILES Code : O=C(C1=NC=C(N2CCN(C(OC(C)(C)C)=O)CC2)N=C1)OC
MDL No. :MFCD12964048

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Application In Synthesis of [ 1215626-40-6 ]

* 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.

  • Downstream synthetic route of [ 1215626-40-6 ]

[ 1215626-40-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1215626-40-6 ]
  • [ 1209646-17-2 ]
YieldReaction ConditionsOperation in experiment
To a stirred suspension of 1-76 (8.60 g, 26.68 mmol) in ethanol (250 ml) is added 5M NaOH (26.68 ml, 133.39 mmol) at room temperature. The mixture becomes homogenous before a persisting precipitate forms and becomes a solid mass. Water (200 ml) is added and the mixture is stirred for 4 h after which time the reaction appears complete. The light brown sludge is poured into a beaker and treated with water. AcOH is added to reach acidic pH and the product is extracted into DCM (2x). The combined organics are dried over anhydrous MgS04, filtered and concentrated to give the product as a solid which is suspended in heptanes. The solid is collected via filtration and washed with heptanes to give 1-77 (7.90 g); m/z 309.4 [M+H].
With water; sodium hydroxide; In ethanol; at 20℃; for 4h; Step 2: Synthesis of 2,3,5,6-Tetrahydro-ri,2'lbipyrazinyl-4,5'-dicarboxylic acid 4-tert- butyl esterR8 (5.0 g, 15.51 mmol) is treated with ethanol (150 ml) and 5N NaOH at room temperature. The mixture becomes homogenous before a persisting precipitate forms. At this time water is added (200 ml) and the resulting solid mass is broken up using a spatula. The reaction is stirred for 4 h and treated with water. The mixture is acidified using acetic acid (AcOH) and the product is extracted into DCM (2x). The combined organics are dried (MgS04), filtered and concentrated to give the title compound. (4.3 g)
With water; sodium hydroxide; In ethanol; for 24h; Step 2: synthesis of 2,3,5,6-Tetrahydro-[l,2']bipyrazinyl-4,5'-dicarboxylic acid 4-tert- butyl ester (R50).R49 (890 mg, 2.76 mmol) is treated with ethanol (25 mL) and 5N NaOH (2.76 mL, 13.8 mmol). The mixture is stirred for several minutes at which time water (approximately 10 mL) is added and the reaction is stirred for 24 hours. The resulting mixture is diluted with water, acidified with acetic acid., and extracted twice with CH2CI2. The combined organic phases are washed with brine, dried over MgS04, filtered, and the solvent is removed in vacuo to afford R50 (690 mg); m/z 309.4 [M+H].
7.90 g With water; sodium hydroxide; In ethanol; for 4h; To a stirred suspension of I-76 (8.60 g, 26.68 mmol) in ethanol (250 ml) is added 5M NaOH (26.68 ml, 133.39 mmol) at room temperature. The mixture becomes homogenous before a persisting precipitate forms and becomes a solid mass. Water (200 ml) is added and the mixture is stirred for 4 h after which time the reaction appears complete. The light brown sludge is poured into a beaker and treated with water. AcOH is added to reach acidic pH and the product is extracted into DCM (2×). The combined organics are dried over anhydrous MgSO4, filtered and concentrated to give the product as a solid which is suspended in heptanes. The solid is collected via filtration and washed with heptanes to give I-77 (7.90 g); m/z 309.4 [M+H].
300 mg With ethanol; sodium hydroxide; In tetrahydrofuran; at 60℃; for 2h; Methyl 5-(4-(tert-butoxycarbonyl) piperazin- 1 -yl) pyrazine-2-carboxylate (2 g, crude) was added into a solution of EtOH (5 ml), THF (5 ml) and NaOH (2 N, 5 ml). The mixture was stirred at 60 C. for 2 h. When the reaction finished, the pH was adjusted to 1 and it was extracted by EA, concentrated to afford the pink solid. (300 mg, 15% yield, 2 steps).

 

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