HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953473Generated: November 1, 2026
1-Bromo-3-chloropropane → HCID 15481567, compound
https://huagongshe.com/reaction/1953473
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Carbonate Ion | HCID 19660 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | HCID 135484041 | HCID 135484041 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15481567 | HCID 15481567 | 47.2% |
Reaction Steps
A mixture of 6-methoxy-3-{2-[3-(2-quinolylmethoxy)benzyl]tetrazolyl}quinolin-2-one (1.00 g, 2.04 mmol), potassium, carbonate (564 mg, 4.08 mmol), 1-bromo-3-chloropropane (962 mg, 6.12 mmol), and DMF (100 ml) was stirred for four hours at a bath temperature of 60° C. The solvent of the reaction mixture was removed under reduced pressure. Water was then added to the mixture, and the mixture was extracted with chloroform-methanol (10:1). The thus-obtained organic phase was dried over magnesium sulfate anhydrate, and the solvent was removed under reduced pressure. The organic phase was then subjected to silica gel column chromatography (developer: chloroform-methanol (100:1)), purified, and crystallized from a chloroform-diethylether mixture, to thereby obtain the title compound (546 mg, 0.963 mmol, 47.2%) as pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06117886 |
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| Source dataset | uspto-grants-2000_09 |
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| ORD ID | ord-cdb19f67ebd0431da58c7ee6b7014985 |
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| Source note | uspto-grants-2000_09 |
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