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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992086Generated: October 25, 2026

Acetic Acid → HCID 178480352, compound

https://huagongshe.com/reaction/992086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(5-fluoro-1-methyl-1H-indol-3-yl)-cyclohexanoneHCID 18414059—
Reactant6-Bromo-8-piperazin-1-yl-quinolineHCID 18414063—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 178480352HCID 178480352—

Reaction Steps

To a solution of 6-bromo-8-piperazin-1-yl-quinoline (610 mg, 2.09 mmol), 4-(5-fluoro-1-methyl-1H-indol-3-yl)-cyclohexanone (510 mg, 2.09 mmol), and sodium triacetoxyborohydride (660 mg, 3.14 mmol) in dichloroethane (40 mL) was added acetic acid (0.24 mL, 4.18 mmol) and stirred overnight at room temperature. The reaction was quenched with 1 M NaOH (50 mL) and H2O (100 mL) then extracted in CH2Cl2 (100 mL) and EtOAc (100 mL). The organic fractions were combined, dried over Na2SO4, concentrated, filtered and chromatographed (5% MeOH/EtOAc). The majority of the cis compound precipitated out of 5% MeOH/EtOAc before application to the column and was purified by filtration affording 510 mg (47%) of the cis isomer as a pale yellow solid: mp 215-217° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06465482B2
Source datasetuspto-grants-2002_10
ORD IDord-c338ce27f5884a1197995610edd2d849
Source noteuspto-grants-2002_10