An update on the compound challenge: 16004-15-2

Compound(16004-15-2)HPLC of Formula: 16004-15-2 received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(1-(Bromomethyl)-4-iodobenzene), if you are interested, you can check out my other related articles.

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Microwave-Assisted Tandem Kornblum Oxidation and Biginelli Reaction for the Synthesis of Dihydropyrimidones, published in 2020-10-19, which mentions a compound: 16004-15-2, mainly applied to dihydropyrimidone dihydro pyrimidinethione preparation green chem microwave irradiation; urea aralkyl bromide ethyl acetoacetate tandem Kornblum Biginelli cyclocondensation; thiourea aralkyl bromide ethyl acetoacetate tandem Kornblum Biginelli cyclocondensation, HPLC of Formula: 16004-15-2.

A simple and straightforward approach for the synthesis of dihydropyrimidones I (X = O, S; Ar = Ph, 4-FC6H4, pyridin-2-yl, 1H-pyrrol-2-yl, etc.) via sequential Kornblum oxidation/Biginelli reaction has been developed. The protocol involves an in situ oxidation of benzyl bromides ArCH2Br which serve as a carbonyl equivalent followed by cyclocondensation with (thio)urea and Et acetoacetate to furnish dihydropyrimidones I under catalyst- and base-free conditions in a one-pot tandem manner under microwave irradiation Further, the product purification using aqueous recrystallization avoids large quantities of volatile and a toxic organic solvent usually required for work-up and significantly less time required for this process makes the method environmentally friendly.

Compound(16004-15-2)HPLC of Formula: 16004-15-2 received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(1-(Bromomethyl)-4-iodobenzene), if you are interested, you can check out my other related articles.

Reference:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics