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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 8-(1-piperazinyl)Quinoline | HCID 11830786 | — |
| Reactant | 1-(7-Methoxy-1-benzofuran-3-yl)propan-2-one | HCID 23614434 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 8-{4-[2-(7-Methoxy-1-benzofuran-3-yl)-1-methylethyl)piperazin-1-yl]quinoline | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07276603B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-c6cea6096bc64987b5e756054faecd5a |
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| Source note | uspto-grants-2007_10 |
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