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Chemical Structure| 1356108-96-7 Chemical Structure| 1356108-96-7

Structure of 1356108-96-7

Chemical Structure| 1356108-96-7

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Product Details of [ 1356108-96-7 ]

CAS No. :1356108-96-7
Formula : C7H9BrClNO2
M.W : 254.51
SMILES Code : BrC1=CN=C(CO)C(CO)=C1.[H]Cl

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Application In Synthesis of [ 1356108-96-7 ]

* 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 [ 1356108-96-7 ]

[ 1356108-96-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 521980-82-5 ]
  • [ 1356108-96-7 ]
YieldReaction ConditionsOperation in experiment
Step B: (5-Bromopyridine-2,3-diyl)dimethanol; Sodium borohydride (15.9 g, 420 mmol) was added portionwise over 30 min to a solution of <strong>[521980-82-5]dimethyl 5-bromopyridine-2,3-dicarboxylate</strong> (20 g, 73 mmol) in ethanol (460 mL) precooled to 0 C. A solution of calcium chloride (23.3 g, 209 mmol) in 150 mL was added slowly at 0 C., and the reaction mixture was warmed to 23 C. and stirred overnight. Excess sodium borohydride was quenched by slow addition of aqueous 2 N HCl solution (230 mL, 460 mmol), followed by a stirring at 23 C. for 2 h. The mixture was concentrated to dryness. Saturated aqueous sodium bicarbonate solution was added to the residue until a pH of approximately 7 was reached. The aqueous mixture was extracted with 2-methyltetrahydrofuran (4×200 mL). The combined organic layers were dried over sodium sulfate then treated with a solution of 4 N HCl in dioxane (25 mL, 100 mmol). The resulting solid was filtered, washed with 2-methyltetrahydrofuran, and dried to give the title compound as a hydrochloride salt. MS: m/z=218.1 (M+1).
Step B: (5-Bromopyridine-2,3-diyl)dimethanol; Sodium borohydride (15.9 g, 420 mmol) was added portionwise over 30 minutes to a solution of <strong>[521980-82-5]dimethyl 5-bromopyridine-2,3-dicarboxylate</strong> (20 g, 73 mmol) in ethanol (460 mL) precooled to 0 C. A solution of calcium chloride (23.3 g, 209 mmol) in ethanol (150 mL) was added slowly at 0 C, and the reaction mixture was warmed to 23 C and stirred overnight. Excess sodium borohydride was quenched by slow addition of aqueous 2 N HC1 solution (230 mL, 460 mmol), followed by a stirring at 23 C for 2 h. The mixture was concentrated to dryness. Saturated aqueous sodium bicarbonate solution was added to the residue until a pH of approximately 7 was reached. The aqueous mixture was extracted with 2-methyltetrahydrofuran (4 x 200 mL). The combined organic layers were dried over sodium sulfate then treated with a solution of 4 N HC1 in dioxane (25 mL, 100 mmol). The resulting solid was filtered, washed with 2-methyltetrahydrofuran, and dried to give the title compound as a hydrochloride salt. MS: mfz = 218.1 (M + 1).
Step B: (5-Bromopyridine-2,3-diyl)dimethanol Sodium borohydride (15.9g, 420 mmol) was added portionwise over 30 min to a solution of <strong>[521980-82-5]dimethyl 5-bromopyridine-2,3-dicarboxylate</strong> (20 g, 73 mmol) in ethanol (460 mL) precooled to 0 C. A solution of calcium chloride (23.3 g, 209 mmol) in 150 mL was added slowly at 0 C, and the reaction mixture was warmed to 23 C and stirred overnight. Excess sodium borohydride was quenched by slow addition of aqueous 2 N HC1 solution (230 mL, 460 mmol), followed by a stirring at 23 C for 2 h. The mixture was concentrated to dryness. Saturated aqueous sodium bicarbonate solution was added to the residue until a pH of approximately 7 was reached. The aqueous mixture was extracted with 2-methyltetrahydrofuran (4 x 200 mL). The combined organic layers were dried over sodium sulfate then treated with a solution of 4 N HC1 in dioxane (25 mL, 100 mmol). The resulting solid was filtered, washed with 2-methyltetrahydrofuran, and dried to give the title compound as a hydrochloride salt. MS: mlz = 218.1 (M + 1).
Step B: (5-Bromopyridine-2,3-diyl)dimethanol Sodium borohydride (15.9 g, 420 mmol) was added portionwise over 30 min to a solution of <strong>[521980-82-5]dimethyl 5-bromopyridine-2,3-dicarboxylate</strong> (20 g, 73 mmol) in EtOH (460 mL) precooled to 0 C. A solution of calcium chloride (23.3 g, 209 mmol) in 150 mL was added slowly at 0 C, and the reaction mixture was warmed to ambient temperature and stirred for 18 h. Excess sodium borohydride was quenched by slow addition of aqueous 2 N HC1 solution (230 mL, 460 mmol), followed by a stirring at ambient temperature for 2 h. The mixture was concentrated to dryness in vacuo. Saturated aqueous sodium bicarbonate solution was added to the residue until a pH of approximately 7 was reached. The aqueous mixture was extracted with 2-methyltetrahydrofuran (4 x 200 mL). The combined organic layers were dried over sodium sulfate then treated with a solution of 4 N HC1 in dioxane (25 mL, 100 mmol). The resulting solid was filtered, washed with 2-methyltetrahydrofuran, and dried to give the title compound as a hydrochloride salt. MS: mlz = 218.1 (M + 1).

 

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