Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042410Generated: November 3, 2026

4-(Piperazin-1-yl)furo[3,2-c]pyridine → HCID 178474979, compound

https://huagongshe.com/reaction/2042410

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Piperazin-1-yl)furo[3,2-c]pyridineHCID 2794808—
ReactantHCID 178474986HCID 178474986—
CatalystMethanolHCID 887—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 178474979HCID 17847497942%

Reaction Steps

To a solution under N2 of commercially available 4-piperazine-1-yl-furo[3,2-c]pyridine [CAS-Nr. 81078-84-4] (125 mg, 0.62 mmol) in 1,2-dichloroethane (1.25 ml) were added trans-N-[4-(2-oxo-ethyl)-cyclohexyl]-acetamide [CAS-Nr. 946599-01-5, WO 2007/093540] (124 mg, 0.68 mmol) and 3 drops of MeOH. The resulting yellow solution was stirred 18 h at room temperature before addition of Na(AcO)3BH (196 mg, 0.92 mmol). After stirring 18 h at room temperature the reaction mixture was partitioned between sat. aq. NaHCO3 sol. (50 ml) and EtOAc (50 ml). The aqueous layer was extracted with more EtOAc (2×25 ml). The combined organic layers were washed with H2O (40 ml) and brine (40 ml) and dried over MgSO4. After evaporation of the solvent, the crude product (yellow crystals) was purified by flash chromatography on silica gel (CH2Cl2/MeOH, 100:0 to 95:5) to yield the title compound as light yellow crystals (95 mg, 42%), MS (ISP) m/z=371.2 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586579B2
Source datasetuspto-grants-2013_11
ORD IDord-579be3c86eb445e4b69d06235a69e541
Source noteuspto-grants-2013_11