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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642208Generated: November 3, 2026

HCID 15952943, compound → N-[2-(3,5-Dichlorophenoxy)phenyl]piperidine-4-carboxamide

https://huagongshe.com/reaction/1642208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15952943HCID 15952943—
Solvent1,4-Dioxane hydrochlorideHCID 20443148—
ProductN-[2-(3,5-Dichlorophenoxy)phenyl]piperidine-4-carboxamideHCID 57550316—

Reaction Steps

4-[2-(3,5-Dichloro-phenoxy)-phenylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl ester (HVB01036, HVB01039 HVB01042, 1.09 g, 2.3 mmol) was dissolved in HCl/dioxane (4M, 18 ml), and stirred at room temperature for 1 h. The reaction mixture was evaporated to dryness, diluted with DCM (20 ml) and neutralised with sodium hydroxide (1M). Extracted with DCM, organic layers dried over anhydrous magnesium sulphate, and evaporated in-vacuo, 183 mg, 21%. m.p. 138-139° C., Rf. 0.3 (10% Methanol/DCM), 1HNMR (CDCl3, 270 MHz) δ 1.65 (3H, m, CH2 and NH), 1.86 (2H, m, CH2), 2.36 (1H, m, CH), 2.65 (2H, td, J=2.7, 9.6 Hz, NCH2), 3.16 (2H, m, NCH2), 6.89 (2H, d, J=1.7 Hz, ArHE, ArHG), 6.90 (1H, m, ArHD), 7.06 (1H, td, J=1.5, 7.4 Hz, ArHB), 7.12 (1H, t, J=1.7 Hz, ArHF), 7.18 (1H, td, J=8.2, 1.46 Hz, ArHC), 7.55 (1H, s, NH), 8.43 (1H, dd, J=8.2 Hz, ArHA).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119627B2
Source datasetuspto-grants-2012_02
ORD IDord-2c0a29fc082841d7b64446bfd51a4eed
Source noteuspto-grants-2012_02