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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1483931Generated: November 1, 2026

Butyric Acid → (S)-2-((1-butyrylpiperidin-3-yl)methoxy)-6-nitrobenzonitrile

https://huagongshe.com/reaction/1483931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyric AcidHCID 264—
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(S)-2-nitro-6-(piperidin-3-ylmethoxy)benzonitrile hydrochlorideHCID 86714270—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product(S)-2-((1-butyrylpiperidin-3-yl)methoxy)-6-nitrobenzonitrileHCID 86714269—

Reaction Steps

To a suspension of (S)-2-nitro-6-(piperidin-3-ylmethoxy)benzonitrile hydrochloride (Example 1d, 9.8 g, 32.92 mmol) in CH2Cl2 (550 mL) and DMF (50 mL) was added triethylamine (9.2 mL, 65.84 mmol). After being stirred at room temperature for 5 min., a solution of butyric acid (3.33 mL, 36.21 mmol), EDCI (6.94 g, 36.21 mmol) and HOBt (4.89 g, 36.21 mmol) in DCM (50 mL) was added, and the reaction mixture was then stirred at room temperature overnight. The resulting mixture was diluted with CH2Cl2, washed with 0.5 N HCl, water, NaHCO3 and brine, dried over MgSO4, filtered and evaporated to give the crude product as a light brown gel, used as this in the next step. MS 332 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09420814B2
Source datasetuspto-grants-2016_08
ORD IDord-5544bb0028a7437eb6994ef665705af4
Source noteuspto-grants-2016_08