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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428566Generated: October 30, 2026

Acetic Acid → HCID 178486623, compound

https://huagongshe.com/reaction/428566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(5-Cyano-1-methyl-3-indolyl)cyclohexanoneHCID 15481282—
Reactant6-Methoxy-8-piperazin-1-yl-[1,7]naphthyridineHCID 18414084—
Solvent1,1-DichloroethaneHCID 6365—
SolventEthyl AcetateHCID 8857—
ProductHCID 178486623HCID 178486623—

Reaction Steps

To a solution of 6-methoxy-8-piperazin-1-yl-[1,7]naphthyridine (250 mg, 1.02 mmol), 4-(5-cyano-1-methyl-1H-indol-3-yl)-cyclohexanone (260 mg, 1.02 mmol), and sodium triacetoxyborohydride (320 mg, 1.53 mmol) in dichloroethane (50 mL) was added acetic acid (0.12 mL, 2.04 mmol) and stirred overnight at room temperature. The reaction was quenched with 1 M NaOH (50 mL) then extracted in CH2Cl2 (1×50 mL) and EtOAc (75 mL). The organic fractions were combined, dried over Na2SO4, concentrated, filtered and chromatographed (5% MeOH/EtOAc+NH4OH) affording 160 mg (33%) of the cis isomer as a yellow foam. The HCl salt was generated form EtOAc affording a pale yellow solid: mp 235-238° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313126B1
Source datasetuspto-grants-2001_11
ORD IDord-f59ce54855c043f4a7a04bdb2997b198
Source noteuspto-grants-2001_11