HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612212Generated: October 26, 2026
Glycol monoethyl ether → 4-(4-Hydroxy-2-methyl-phenylamino)-6-methoxy-7-(3-morpholin-4-yl-propoxy)-quinoline-3-carbonitrile
https://huagongshe.com/reaction/612212
Participants
| Role | Name | HCID | Charge |
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| Reactant | Glycol monoethyl ether | HCID 8076 | — |
| Reactant | 4-Amino-m-cresol | HCID 17819 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Reactant | 4-Chloro-6-methoxy-7-(3-morpholinopropoxy)quinoline-3-carbonitrile | HCID 22466601 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(4-Hydroxy-2-methyl-phenylamino)-6-methoxy-7-(3-morpholin-4-yl-propoxy)-quinoline-3-carbonitrile | HCID 22466690 | 61.8% |
Reaction Steps
A mixture of 0.3 g of 4chloro-6-methoxy-7-(3-morpholin-4-yl-propoxy)-quinoline-3-carbonitrile derivative, 0.12 g of 4amino-m-cresol, 0.1 g of pyridine hydrochloride and 4 ml of 2-ethoxy ethanol was stirred under nitrogen at reflux temperature for 1.5 hr. The mixture was cooled and added to the mixture of ethyl acetate and saturated solution of sodium bicarbonate, stirred for 15 minutes. Following separation of layers, the organic layer was dried over anhydrous sodium sulfate, filtered and filtrate was evaporated to yield dark oil. The oil was purified by silica gel flash chromatography utilizing a gradient of methylene chloride/methanol (95:5 to 90:10 ) to give 0.23 g of the title compound as a tan solid, mp120-126 C; mass spectrum (electrospray, m/e):M+H 449.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06002008 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-f1670b9cd6974024861328f172222743 |
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| Source note | uspto-grants-1999_12 |
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