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  2. Pyrrole - Wikipedia

    en.wikipedia.org/wiki/Pyrrole

    Pyrrole is an extremely weak base for an amine, with a conjugate acid pK a of −3.8. The most thermodynamically stable pyrrolium cation (C 4 H 6 N + ) is formed by protonation at the 2 position. Substitution of pyrrole with alkyl substituents provides a more basic molecule—for example, tetramethylpyrrole has a conjugate acid p K a of +3.7.

  3. Hantzsch pyrrole synthesis - Wikipedia

    en.wikipedia.org/wiki/Hantzsch_pyrrole_synthesis

    Below is one published mechanism for the reaction: [5] Mechanism for the Hantzsch Pyrrole Synthesis. The mechanism starts with the amine (1) attacking the β carbon of the β-ketoesters (2), and eventually forming an enamine (3). The enamine then attacks the carbonyl carbon of the α-haloketone (4).

  4. Knorr pyrrole synthesis - Wikipedia

    en.wikipedia.org/wiki/Knorr_pyrrole_synthesis

    The Knorr pyrrole synthesis is a widely used chemical reaction that synthesizes substituted pyrroles (3). [1] [2] [3] The method involves the reaction of an α-amino-ketone (1) and a compound containing an electron-withdrawing group (e.g. an ester as shown) α to a carbonyl group (2). [4] The Knorr pyrrole synthesis

  5. Pyrroline - Wikipedia

    en.wikipedia.org/wiki/Pyrroline

    Pyrrolines, also known under the name dihydropyrroles, are three different heterocyclic organic chemical compounds that differ in the position of the double bond.Pyrrolines are formally derived from the aromate pyrrole by hydrogenation. 1-Pyrroline is a cyclic imine, whereas 2-pyrroline and 3-pyrroline are cyclic amines.

  6. Paal–Knorr synthesis - Wikipedia

    en.wikipedia.org/wiki/Paal–Knorr_synthesis

    The amine attacks the other carbonyl to form a 2,5-dihydroxytetrahydropyrrole derivative which undergoes dehydration to give the corresponding substituted pyrrole. [7] Paal–Knorr pyrrole synthesis mechanism. The reaction is typically run under protic or Lewis acidic conditions, with a primary amine.

  7. Enamine - Wikipedia

    en.wikipedia.org/wiki/Enamine

    Primary amines are usually not used for enamine synthesis due to the preferential formation of the more thermodynamically stable imine species. [11] Methyl ketone self-condensation is a side-reaction which can be avoided through the addition of TiCl 4 [12] into the reaction mixture (to act as a water scavenger).

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  9. Porphobilinogen - Wikipedia

    en.wikipedia.org/wiki/Porphobilinogen

    [1] The structure of the molecule can be described as molecule of pyrrole with sidechains substituted for hydrogen atoms at positions 2, 3 and 4 in the ring (1 being the nitrogen atom); respectively, an aminomethyl group −CH 2 −NH 2, an acetic acid (carboxymethyl) group −CH 2 −COOH, and a propionic acid (carboxyethyl) group −CH 2 − ...