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  2. Hydrazide - Wikipedia

    en.wikipedia.org/wiki/Hydrazide

    An applied example is a synthesis of sunitinib begins by mixing 5-fluoroisatin slowly into hydrazine hydrate. [9] After 4 hours at 110 °C, the indole ring structure has been broken into (2-amino-5-fluoro-phenyl)-acetic acid hydrazide with reduction of the ketone at the 3-position.

  3. Hydrazine - Wikipedia

    en.wikipedia.org/wiki/Hydrazine

    Hydrazine is an inorganic compound with the chemical formula N 2 H 4.It is a simple pnictogen hydride, and is a colourless flammable liquid with an ammonia-like odour.Hydrazine is highly hazardous unless handled in solution as, for example, hydrazine hydrate (N 2 H 4 ·xH 2 O).

  4. Hydrazines - Wikipedia

    en.wikipedia.org/wiki/Hydrazines

    Hydrazines (R 2 N−NR 2) are a class of chemical compounds with two nitrogen atoms linked via a covalent bond and which carry from one up to four alkyl or aryl substituents. . Hydrazines can be considered as derivatives of the inorganic hydrazine (H 2 N−NH 2), in which one or more hydrogen atoms have been replaced by hydrocarbon grou

  5. Hydrazone - Wikipedia

    en.wikipedia.org/wiki/Hydrazone

    When derived from hydrazine itself, hydrazones condense with a second equivalent of a carbonyl to give azines: [10] R 2 C=N−NH 2 + R 2 C=O → R 2 C=N−N=CR 2 + H 2 O. Hydrazones are intermediates in the Wolff–Kishner reduction. Hydrazones are reactants in hydrazone iodination, the Shapiro reaction, and the Bamford–Stevens reaction to ...

  6. Carbohydrazide - Wikipedia

    en.wikipedia.org/wiki/Carbohydrazide

    Industrially the compound is produced by treatment of urea with hydrazine: [3] OC(NH 2) 2 + 2 N 2 H 4 → OC(N 2 H 3) 2 + 2 NH 3. It can also be prepared by reactions of other C1-precursors with hydrazine, such as carbonate esters. [2] It can be prepared from phosgene, but this route cogenerates the hydrazinium salt [N 2 H 5]Cl and results in ...

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  8. Pellizzari reaction - Wikipedia

    en.wikipedia.org/wiki/Pellizzari_reaction

    The Pellizzari reaction was discovered in 1911 by Guido Pellizzari, and is the organic reaction of an amide and a hydrazide to form a 1,2,4-triazole. [1] The product is similar to that of the Einhorn-Brunner reaction, but the mechanism itself is not regioselective. An overview of the Pellizzari reaction

  9. Dying To Be Free - The Huffington Post

    projects.huffingtonpost.com/dying-to-be-free...

    That day, in August 2013, Patrick got in the car and put the duffel bag on a seat. Inside was a talisman he’d been given by the treatment facility: a hardcover fourth edition of the Alcoholics Anonymous bible known as “The Big Book.”