HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635075Generated: October 27, 2026
Water → 9-Hydroxy-9,12-dihydro-7H-cyclopenta[6,7]indolizino[1,2-b]-quinoline-7,10(8H)-dione
https://huagongshe.com/reaction/1635075
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | 2-Bromo-3-(bromomethyl)quinoline | HCID 613324 | — |
| Reactant | dimethoxyethane N,N-dimethylformamide | HCID 18463208 | — |
| Product | 9-Hydroxy-9,12-dihydro-7H-cyclopenta[6,7]indolizino[1,2-b]-quinoline-7,10(8H)-dione | HCID 9882915 | — |
Reaction Steps
0.6 mmol (18 mg) of NaH as an 80% dispersion in mineral oil is added in small fractions to a solution, stirred at 0° C., of 0.6 mmol (100 mg) of the compound described in Preparation A in 20 ml of a DME/DMF mixture (16/4 (v/v)). The mixture is stirred at 0° C. for 10 minutes before the addition, at that temperature, of 2.4 mmol (210 mg) of LiBr. After returning to room temperature, the reaction mixture is stirred for ¼ hour before the addition of 0.66 mmol (200 mg) of 2-bromo-3-bromomethylquinoline. The reaction mixture is then heated at 80° C. for 20 hours and, after returning to room temperature, subsequently poured into a large excess of water. The precipitate that forms is filtered off and washed with ether to yield the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06509345B2 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-8ef1e457b7454c29911682cc82bda246 |
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| Source note | uspto-grants-2003_01 |
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