Carboxamides N-

Furan-3-carboxamide, N,fV-dimethyl-AG, 4, 34 <76JOC3591, 77TI337) Furan-2-carboxylate, 2-nitro-, ethyl ester UV, 4, 588 <50JA753>... [Pg.24]

Pyrrole-2-carboxamide, N,N-dimethyl-conformation, 4, 194 Pyrrole-3-carboxamide, N,N-dimethyl-conformation, 4, 194 Pyrrolecarboxamides synthesis, 4, 242 Pyrrole-2-carboxamides synthesis, 4, 148, 360 Pyrrolecarboxylhydrazides Curtius degradation, 4, 362 Pyrrole-2-carboxylic acid, l-benzyl-3-hydroxy-ethyl ester... [Pg.817]

Mixed donor ligands. The complex [FeL3]Cl3 (L = acetylhydrazine) contains the ligand in its bidentate form, bonded via the carbonyl and primary amino-groups.Pyridine-2-carboxaldehyde and l,l,l-tris(aminoethyl)ethane react with Fe" via a template reaction to form [Fejlpyljltame) ], in which three molecules of carboxaldehyde have condensed with one molecule of triamine to produce (pyljltame). MeC(CH2N=CH-oc-py)3 the complex cation is octahedral. The complexes [FeL ] (L = l,10-phenanthroline-2-carboxamide, n = 1 or 2) have been isolated they are both six-co-ordinate. Very weak d-d bands have been identified in the spectra of complexes of ot-picolinic acid and quinaldic acid with Fe". ... [Pg.220]

NORLYSERGIC ACID, N,N-DIETHYLAMIDE 6-ETHYL 6-NORLYSERGAMIDE, N,N-DIETHYL-6-ETHYL N,N-DIETHYLNORLYSERGAMIDE, 6-ETHYL N-(6)-ETHYLNORLYSERGIC ACID, N,N-DIETHYLAMIDE 9,10-DIDEHYDRO-N,N,6-TRIETHYLERGOLINE-8b-CARBOXAMIDE N-ETHYL-NOR-LSD... [Pg.87]

This procedure illustrates a general method for preparing aliphatic and, in certain cases, aromatic /3-lactarns containing a free NH group and substituted in either the 4 position or in both the-3 and 4 positions of the 2-azetidinone ring. The major byproduct of the cycloaddition step is a /3,7-unsaturated carbox-amide-N-sulfonyl chloride which, in the case of certain aromatic olefins, may predominate. Reactions of both /3-lactam-N-sulfonyl chlorides and the /3,y-unsaturated carboxamide-N-sulfonyl chlorides have been tabulated.3... [Pg.56]

H NMR, 4, 557, 566 <75CS(7)211> Furan-2-carboxamide dipole moment, 4, 555 (B-63MI31000) Furan-2-carboxamide, N, N-dimethyl-ACrnt, 4, 34 (76JOC3591, 77TI337)... [Pg.24]

H-Pyrrole-2-carboxamide, N.N-dimethyl-AGrot, 4, 34 <76JOC3591, 77X1337), 194 <76JOC3591>... [Pg.55]

Selenophene-2-carboxamide, N,iV-dimethyl-PE, 4, 25 (76JCS(P2)276> Selenophene-2-carboxylic acid microwave, 4, 4, 937 (62AX737) pX 4, 71 (77AHC(21)119)... [Pg.58]

N1 -Carboxamide-N-Guanyi Triazene [Triazendi-carbon saureamid-amidin (Ger)] H2N.CO.N N.NH.C( NH).NH2+H2 Of C2H8N602 mw 132.16 N 63.60% OB to C02 +24.21% yel ndles (from hot w) mp, decomps explosively at 95°, puffs off at 139° on rapid heating. V sol in alkalies si sol in w. Prepn is by gently warming N-aminoim inome thy 1- N-carb onic acid ethyl ester-triazene with ammonia. The compd forms expl salts such as the Hydrochloride, C2H6N60+HC1 mw 167.09 N 50.31% ... [Pg.844]

Chemical Name Tricyclo[3.3.1.13,7]decane-l-carboxamide, N-(2-(4-(2-pyrimidinyl)-l-piperazinyl)ethyl)-, hydrochloride... [Pg.100]

Chemical Name Ergoline-8-carboxamide, N-cyclohexyl-6-methyl-l-(l-methylethyl)-, (8(3)-... [Pg.239]

Small quantities of the 5-amino-4-imidazolecarboxamide nucleotide were also isolated from the culture medium of Escherichia coli grown under sulfonamide bacteriostasis.i i This substance is considered to be an intermediate in purine biosynthesis, both in micro-organisms and in mammalian cells. In sulfonamide-inhibited cells and in the purine-requiring mutant of Escherichia coli, there is a block in the conversion of 5-amino-4-imidazole-carboxamide n-ribonucleotide to inosinic acid. The accumulated nucleotide in the bacterial cell is probably attacked by phosphatases this would explain why the nucleoside is the main metabolite. [Pg.222]

H-CYCLOHEPTA(b)QUINOLINE-ll-CARBOXAMIDE, N,N-DIETHYL-7,8,9,10-TETRAHYDRO- see TCOlOO 6H-CYCLOHEPTA(b)QUINOLINE, 7,8,9,10-TETRAHYDRO-1 l-(MORPHOLINOCARBONYL)- see MRU077... [Pg.1599]

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