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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178827Generated: October 26, 2026

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

https://huagongshe.com/reaction/1178827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant8-(1-piperazinyl)QuinolineHCID 11830786—
Reactant1-(7-Methoxy-1-benzofuran-3-yl)propan-2-oneHCID 23614434—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
Product8-{4-[2-(7-Methoxy-1-benzofuran-3-yl)-1-methylethyl)piperazin-1-yl]quinolineHCID 11165528—

Reaction Steps

To a stirred mixture of 1-(7-methoxy-1-benzofuran-3-yl)acetone (204 mg, 1 mmol) and 8-piperazino quinoline (213.0 mg, 1 mmol) in 1,2-dichloroethane (100 ml) and acetic acid (1 ml), sodium triacetoxyborohydride (422 mg, 2 mmol) was added at room temperature. Reaction mixture was stirred at room temperature for 72 hrs. At the end, the reaction mixture was neutralized with 10% NaHCO3 and extracted with chloroform. The organic layer was dried over anhydrous MgSO4, filtered and concentrated. The product obtained 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 yellow oil. Yield: 60 mg (14%); (M+H): 402; 1HNMR (400 MHz, CDCl3): δ 8.90˜8.14 (dd, J1=1.8 Hz, J2=1.8 Hz, 1H); 8.13˜7.56 (dd, J1=1.8 Hz, J2=1.8 Hz, 1H); 7.46˜6.80 (m, 8H); 4.01 (s, 3H); 3.51˜1.60 (m, 11H); 1.14(d, J=6.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276603B2
Source datasetuspto-grants-2007_10
ORD IDord-c6cea6096bc64987b5e756054faecd5a
Source noteuspto-grants-2007_10