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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806550Generated: October 26, 2026

4-Amino-2,2,6,6-tetramethylpiperidine → N-(3-{8-(2,6-difluorophenyl)-7-oxo-2-[(2,2,6,6-tetramethyl-4-piperidinyl)amino]-7,8-dihydropyrido[2,3-d]pyrimidin-4-yl]-4-methylphenyl)-3-thiophenecarboxamide

https://huagongshe.com/reaction/1806550

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-2,2,6,6-tetramethylpiperidineHCID 37524—
ReactantN-{3-[8-(2,6-difluorophenyl)-2-(methylsulfonyl)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidin-4-yl]-4-methylphenyl}-3-thiophenecarboxamideHCID 11947980—
SolventAcetonitrileHCID 6342—
ProductN-(3-{8-(2,6-difluorophenyl)-7-oxo-2-[(2,2,6,6-tetramethyl-4-piperidinyl)amino]-7,8-dihydropyrido[2,3-d]pyrimidin-4-yl]-4-methylphenyl)-3-thiophenecarboxamideHCID 1194798116%

Reaction Steps

The title compound was prepared from N-{3-[8-(2,6-difluorophenyl)-2-(methylsulfonyl)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidin-4-yl]-4-methylphenyl}-3-thiophenecarboxamide and 2,2,6,6-tetramethyl-4-piperidinamine according to General Procedure for Sulfoxide/Sulfone Displacement, described above. The concentrated reaction mixture was slurried with acetonitrile and filtered. The solid was recrystallized from methanol/water to afford the desired product as a crystalline solid (0.2 g, 16%). HPLC indicated >99% pure: LC-MS m/z 629 (M+H)+, 1.86 min (ret time).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354416B2
Source datasetuspto-grants-2013_01
ORD IDord-315391da08054374b6839e9046302d5f
Source noteuspto-grants-2013_01