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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517536Generated: October 28, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 1-[2-(2-Benzyloxypyridin-3-yl)-4-tert-butyl-5-methoxybenzoyl]piperidine-4-carbonitrile

https://huagongshe.com/reaction/1517536

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantPiperidinocarbonitrileHCID 73736—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(2-Benzyloxypyridin-3-yl)-4-tert-butyl-5-methoxybenzoic acidHCID 67374411—
SolventDimethylformamideHCID 6228—
Product1-[2-(2-Benzyloxypyridin-3-yl)-4-tert-butyl-5-methoxybenzoyl]piperidine-4-carbonitrileHCID 67374249100.2%

Reaction Steps

step 4—To a solution of 68 (100 mg, 0.26 mmol) in DMF (3 mL) were added 4 cyano-piperidine (32 mg, 0.29 mmol), HOBt (39 mg, 0.29 mmol), EDCI (56 mg, 0.29 mmol) and DIPEA. The reaction mixture was stirred at RT overnight then quenched with H2O and thrice extracted with EtOAc. The combined extracts were sequentially washed with H2O (3 times) and brine, dried (MgSO4), filtered and concentrated under reduced pressure to afford 126 mg (99%) of 1-[2-(2-benzyloxypyridin-3-yl)-4-tert-butyl-5-methoxybenzoyl]piperidine-4-carbonitrile (70) as a pale yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232271B2
Source datasetuspto-grants-2012_07
ORD IDord-58e11924eb374a5a96a06756f90e6b75
Source noteuspto-grants-2012_07