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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280119Generated: November 1, 2026

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

https://huagongshe.com/reaction/2280119

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 numberUS09138013B2
Source datasetuspto-grants-2015_09
ORD IDord-652a0c0e94e54fe2bbbcbdb9ad50a86b
Source noteuspto-grants-2015_09