Piperidylthiambutene (Piperidinohton) is a synthetic
opioid
Opioids are a class of Drug, drugs that derive from, or mimic, natural substances found in the Papaver somniferum, opium poppy plant. Opioids work on opioid receptors in the brain and other organs to produce a variety of morphine-like effects, ...
analgesic
An analgesic drug, also called simply an analgesic, antalgic, pain reliever, or painkiller, is any member of the group of drugs used for pain management. Analgesics are conceptually distinct from anesthetics, which temporarily reduce, and in s ...
drug from the
thiambutene family, which has around the same potency as
morphine
Morphine, formerly also called morphia, is an opiate that is found naturally in opium, a dark brown resin produced by drying the latex of opium poppies (''Papaver somniferum''). It is mainly used as an analgesic (pain medication). There are ...
. Piperidylthiambutene is structurally distinct from
fentanyl
Fentanyl is a highly potent synthetic piperidine opioid primarily used as an analgesic (pain medication). It is 30 to 50 times more Potency (pharmacology), potent than heroin and 50 to 100 times more potent than morphine. Its primary Medici ...
, its analogues, and other synthetic
opioids
Opioids are a class of Drug, drugs that derive from, or mimic, natural substances found in the Papaver somniferum, opium poppy plant. Opioids work on opioid receptors in the brain and other organs to produce a variety of morphine-like effects, ...
previously reported.
If sold or obtained for the purpose of human consumption it could be considered a
controlled substance analogue in some countries such as the US, Australia and New Zealand. Piperidylthiambutene has been sold as a
designer drug
A designer drug is a structural or functional analog of a controlled substance that has been designed to mimic the pharmacological effects of the original drug, while avoiding classification as illegal and/or detection in standard drug tests. ...
, first appearing in late 2018.
Synthesis

The Grignard reaction between 3-Piperidinobutyric acid ethyl ester
CID:10774378(1) and 2-Bromothiophene
003-09-4(2) gives 3. Dehydration in acid completes the synthesis.
References
Opioids
Thiophenes
1-Piperidinyl compounds
Mu-opioid receptor agonists
{{analgesic-stub