تفاعل #79153

ord-816abe7237094fe3ac23eee9419270c4

معادلة التفاعل

C(=Cc1nc2ccccc2[nH]1)c1ccccc1
2-styryl-1H-benzimidazole
Clc1cccc(Cl)n1
2,6-dichloropyridine
C(=C\c1nc2ccccc2n1-c1ccccn1)/c1ccccc1
(E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole
Clc1cccc(-n2c(/C=C/c3ccccc3)nc3ccccc32)n1
titled compound
Clc1cccc(-n2c(/C=C/c3ccccc3)nc3ccccc32)n1
(E)-1-(6-Chloropyridin-2-yl)-2-styryl-1H-benzimidazole

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

الإجراء التجريبي

Free base of the titled compound was prepared from 2-styryl-1H-benzimidazole and 2,6-dichloropyridine according to the preparation of (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole (Example 1, method B). MW: 331.81; mp: 122.0-123.0° C.; 1H-NMR (DMSO) δ: 8.22 (1H, t, J=7.9 Hz), 7.91 (1H, d, J=16.1 Hz), 7.79-7.72 (3H, m), 7.67-7.63 (2H, m), 7.50-7.47 (1H, m), 746-7.28 (5H, m), 7.23 (1H, d, J=16.1 Hz).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06713482B2uspto-grants-2004_03