Synthesis of 2-methylpyrido (3,2-e) pyrrolo (1,2-a) pyrazine.
نویسندگان
چکیده
منابع مشابه
N′-[(E)-2-Methoxybenzylidene]pyrazine-2-carbohydrazide
In the title compound, C(13)H(12)N(4)O(2), all the non-H atoms lie on a crystallographic mirror plane and an intra-molecular N-H⋯N hydrogen bond generates an S(5) ring; the conformation about the imine bond [1.280 (3) Å] is E. In the crystal, mol-ecules assemble into a two-dimensional array via C-H⋯O(carbon-yl) and C-H⋯N(pyrazine) contacts. Layers stack along the b-axis direction via weak π-π i...
متن کاملN′-[(E)-2,6-Dichlorobenzylidene]pyrazine-2-carbohydrazide
The title compound, C(12)H(8)Cl(2)N(4)O, is non-planar, the dihedral angle formed between the pendant pyrazine and benzene rings being 12.55 (11)°. An intra-molecular N-H⋯N hydrogen bond occurs. The amide groups self-associate via N-H⋯O hydrogen bonding, forming supra-molecular chains with base vector [101], which are stabilized by C-H⋯O contacts. C-H⋯N inter-actions are formed orthogonal to th...
متن کاملN′-[(E)-4-Bromobenzylidene]pyrazine-2-carbohydrazide
In the title compound, C12H9BrN4O, the N'-methyl-idene-pyrazine-2-carbohydrazide and 4-bromobenzene groups are oriented at a dihedral angle of 10.57 (7)°. The hydrazide N-H group is involved in intra-molecular N-H⋯N inter-action, which generates an S(5) motif. A short C-H⋯O inter-action is formed between the methyl-idene H atom and the carbonyl O atom. It connects mol-ecules into chains extendi...
متن کاملN′-[(E)-3-Bromobenzylidene]pyrazine-2-carbohydrazide
In the title compound, C12H9BrN4O, the dihedral angle between the aromatic rings is 12.16 (12)°. An intra-molecular N-H⋯N hydrogen bond closes an S(5) ring. In the crystal, C-H⋯O hydrogen bonds link the mol-ecules into C(6) chains propagating in [010]. Very weak aromatic π-π stacking [centroid-centroid separations = 3.9189 (15) and 3.9357 (15) Å] is also observed.
متن کاملSimple synthesis of pyrrolo[3,2-e]indole-1-carbonitriles
Alkylation of 5-nitroindol-4-ylacetonitriles with ethyl chloroacetate, α-halomethyl ketones, and chloroacetonitrile followed by a treatment of the products with chlorotrimethylsilane in the presence of DBU gives 1-cyanopyrrolo[3,2-e]indoles substituted in position 2 with electron-withdrawing groups.
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Chemical and Pharmaceutical Bulletin
سال: 1985
ISSN: 0009-2363,1347-5223
DOI: 10.1248/cpb.33.4242