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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220977Generated: October 30, 2026

Diisopropylethylamine → 1-(3,3-Dimethyl-butyl)-piperidine-4-carboxylic Acid 4-[(4-chloro-phenyl)-methyl-carbamoyl]-2-methyl-benzylamide

https://huagongshe.com/reaction/220977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant1-(3,3-Dimethylbutyl)piperidine-4-carboxylic acidHCID 23112378—
Reactant4-Aminomethyl-N-(4-chloro-phenyl)-3,N-dimethyl-benzamideHCID 57555220—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-(3,3-Dimethyl-butyl)-piperidine-4-carboxylic Acid 4-[(4-chloro-phenyl)-methyl-carbamoyl]-2-methyl-benzylamideHCID 5755542883%

Reaction Steps

HBTU (296 mg, 0.78 mmol) was added to a solution of 1-(3,3-dimethyl-butyl)-piperidine-4-carboxylic acid from Example E15 (182 mg, 0.73 mmol) in DMF (5 ml) and DIEA (0.272 ml, 1.56 mmol). The mixture was stirred at room temperature for 2 h then 4-aminomethyl-N-(4-chloro-phenyl)-3,N-dimethyl-benzamide from Example E115.2 (150 mg, 0.52 mmol) was added. The mixture was stirred for 2 h at room temperature then diluted with EtOAc, washed with saturated NaHCO3 then brine, dried and concentrated in vacuo. The residue was purified by preparative HPLC (eluant; 0.5% 35% ammonia:9.5% methanol:90% dichloromethane) to give a white powder identified as the title compound (209 mg, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202858B2
Source datasetuspto-grants-2012_06
ORD IDord-6bc183089b3143d18b804a2044101a58
Source noteuspto-grants-2012_06