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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178828Generated: October 26, 2026

Sodium triacetoxyborohydride → 6-Methoxy-8-{4-[2-(7-methoxy-1-benzofuran-3-yl)-1-methylethyl)piperazin-1-yl]quinoline

https://huagongshe.com/reaction/1178828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant6-Methoxy-8-(piperazin-1-YL)quinolineHCID 18414177—
Reactant1-(7-Methoxy-1-benzofuran-3-yl)propan-2-oneHCID 23614434—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
Product6-Methoxy-8-{4-[2-(7-methoxy-1-benzofuran-3-yl)-1-methylethyl)piperazin-1-yl]quinolineHCID 11339439—

Reaction Steps

6-methoxy-8-{4-[2-(7-methoxy-1-benzofuran-3-yl)-1-methylethyl)piperazin-1-yl]quinoline was prepared by generally following the procedure outlined in example 35, step 2, starting from the 1-(7-methoxy-1-benzofuran-3-yl)acetone (204 mg, 1 mmol) and 6-methoxy-8-piperazino quinoline (243.0 mg, 1 mmol) in 1,2-dichloroethane (100 ml) and acetic acid (1 ml), sodium triacetoxyborohydride (422 mg, 2 mmol). The product was purified by silica-gel column chromatography by eluting it initially with 80% ethyl acetate:hexane and then with 5% methanol:ethyl acetate, yielding a brown semi-solid. Yield: 75 mg (17%); (M+H): 432.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276603B2
Source datasetuspto-grants-2007_10
ORD IDord-be888245b4984c509d9499d6c40867c1
Source noteuspto-grants-2007_10