Synthesis of 1-(2-Pyridyl) amino-3-<i>o</i>-tolyloxy-2-propanol
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منابع مشابه
Inhibition of choline synthesis in young rats by 2-amino-2-methyl-propanol-1.
2-Amino-2-methylpropanol-1 and LY ,a-dimethyltriethylcholine have been found to be competitive inhibitors of choline utilization in 40 to 50 gm. male albino rats (1). The former substance apparently only antagonized the utilization of choline in the kidney’ while the latter was an antimetabelite both in the liver and kidney. The quantitative relationships between these inhibitors and choline in...
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A few analogues of atevirdine or 1-[(5-methoxyindol-2-yl) carbonyl]-4-[3- (ethylamino)-2-pyridyl] piperazine – an anti-HIV belonging to non-nucleoside reverse transcriptase inhibitors were synthesized and evaluated for anti-HIV activity. Replacement of indolyl moiety with 2-alkylthio-1-benzyl-5-imidazolyl substituent afforded 1-[2-(alkylthio-1-benzyl-5-imidazolyl) carbonyl]-4-[3-(isopropylamino...
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The title azaazulene 3 was synthesized either by reaction of tropone with N-{(2-pyridyl)acetyl}pyridinium iodide in the presence of ammonium acetate or by palladium-catalyzed cross-couplings between 2-halo-1-azaazulene and 2-substituted pyridine. The compound shows relatively stronger basicity compared with 2,2’-bipyridyl. While 3 showed no emission from the S1 state but from the S2 state like ...
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The syntheses of the title compounds are described. 1- [[2- Amino -1 - (hydroxymethyl) ethoxy] methyl] uracil exhibitslittleactivity against herpesviruses (HSV) in vivo
متن کامل(3-Aminophenyl)diphenylphosphine oxide–2-propanol (1/1)
The title compound, C(18)H(16)NOP·C(3)H(8)O, was synthesized by the reduction of (3-nitro-phen-yl)diphenyl-phosphine oxide in the presence of 2-propanol as recrystallization solvent. There are two molecules in the asymmetric unit. Each P atom is tetra-coordinated by three C and one O atom from two phenyl fragments, one aniline group and one double-bonded O atom in a distorted tetra-hedral geome...
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ژورنال
عنوان ژورنال: YAKUGAKU ZASSHI
سال: 1962
ISSN: 0031-6903,1347-5231
DOI: 10.1248/yakushi1947.82.5_769