HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974063Generated: October 29, 2026
2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline → HCID 14856084, compound
https://huagongshe.com/reaction/974063
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline | HCID 27833 | — |
| Reactant | HCID 9898994 | HCID 9898994 | — |
| Reactant | HCID 69648672 | HCID 69648672 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14856084 | HCID 14856084 | 22.5% |
Reaction Steps
A solution of 4-chloro-2-(Z)-methoxyimino-3-oxo-butanoic acid (4.05 g, 22.6 mmol.), diphenylmethyl 7-amino-3-[(1,2,3-thiadiazol-5-yl)thiomethyl]ceph-3-em-4-carboxylate (11.2 g, 22.6 mmol.) and 1-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (5.58 g, 22.6 mmol.) in 200 ml of methylene chloride was stirred at room temperature for 3 hours. The solution was evaporated to dryness at reduced pressure and the residue was taken up in 150 ml of ethyl acetate which was extracted with 50 ml aliquots of 1N hydrochloric acid, water, saturated sodium bicarbonate, water and brine. The ethyl acetate was dried over magnesium sulfate, evaporated to dryness and the resulting product was purified by flash chromatography on silica gel 60 using ethyl acetate:hexane (1:2) as the eluent to afford 3.34 g of the desired compound:NMR (CDCl3) δ3.52 (pair of d, 2H, J=18 Hz, endocyclic --CH2S--), 4.05 (pair of d, 2 H, J=13 Hz, exocyclic --CH2S--), 4.15 (S, 3H, --OCH3) j, 4.59 (S, 2H, ClCH2 --), 5.04 (d, 1H, J=4.7 Hz, 6H of 7ACA), 5.88 (dd, 1H, J=4.7 and 8.6 Hz, 7H of 7ACA), 6.89 (S, 1H, --CH--), 7.33 (m, 10H, aromatic H), 8.37 (S, 1H, thiadiazole H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05066799 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-26c1adb9de66440c815420aafe28f7b2 |
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| Source note | uspto-grants-1991_11 |
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