SELECTIVE MONO BROMINATION OF 1,4-DIHYDROPYRIDINES

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MIRZAEI Y.R.; ZENOUZ A.M.

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Journal Paper

Paper Information

Journal: Iranian Journal of Chemistry and Chemical Engineering Year:1997 | Volume:16 | Issue:1 Page(s): 29-32

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Information Journal Paper

Title

SELECTIVE MONO BROMINATION OF 1,4-DIHYDROPYRIDINES

Author(s)

MIRZAEI Y.R. | ZENOUZ A.M.

Keywords

NIFEDIPINE ANALOGUES; CALCIUM CHANNEL ANTAGONIST; 2

4-DIHYDROPYRIDINES; BROMOMETHYL-1

4-DIHYDROPYRIDINES

Abstract

2-monobromomethyl 1,4-DIHYDROPYRIDINES is selectively synthesized by bromination of the parent compound by 1.1 equivalents of pyridinium bromide perbromide in dichloromethane/pyridine at -20 degrees C. The same reagent in dichloromethane at 0 degrees C produce the 2,6-bis(bromomethyl) 1,4-DIHYDROPYRIDINES.

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APA: Copy

MIRZAEI, Y.R., & ZENOUZ, A.M.. (1997). SELECTIVE MONO BROMINATION OF 1,4-DIHYDROPYRIDINES . IRANIAN JOURNAL OF CHEMISTRY AND CHEMICAL ENGINEERING (IJCCE), 16(1), 29-32. SID. https://sid.ir/paper/539904/en

Vancouver: Copy

MIRZAEI Y.R., ZENOUZ A.M.. SELECTIVE MONO BROMINATION OF 1,4-DIHYDROPYRIDINES . IRANIAN JOURNAL OF CHEMISTRY AND CHEMICAL ENGINEERING (IJCCE)[Internet]. 1997;16(1):29-32. Available from: https://sid.ir/paper/539904/en

IEEE: Copy

Y.R. MIRZAEI, and A.M. ZENOUZ, “SELECTIVE MONO BROMINATION OF 1,4-DIHYDROPYRIDINES ,” IRANIAN JOURNAL OF CHEMISTRY AND CHEMICAL ENGINEERING (IJCCE), vol. 16, no. 1, pp. 29–32, 1997, [Online]. Available: https://sid.ir/paper/539904/en

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