HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728549Generated: October 29, 2026
3-Butyryl-4-chloro-8-methoxyquinoline → HCID 14989684, compound
https://huagongshe.com/reaction/728549
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Butyryl-4-chloro-8-methoxyquinoline | HCID 11777567 | — |
| Reactant | 3-Methylthiophen-2-amine | HCID 14536436 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 14989684 | HCID 14989684 | 36.4% |
Reaction Steps
3-Butyryl-4-chloro-8-methoxyquinoline (3.6 g, 0.0137 mol) and 2-amino-3-methylthiophene (3.4 g, 0.03 mol) in 1,4 dioxan (30 ml) under a nitrogen atmosphere were stirred at room temperature for 20 hours. The solvent was evaporated under reduced pressure to give an oil. The oil was taken up in dichloromethane and extracted with 2N hydrochloric acid (3×100ml). The dichloromethane extracts were then washed with sodium carbonate solution (100 ml), dried over magnesium sulphate, filtered and evaporated under reduced pressure to give a solid. The solid was purified by flash chromatography using a gradient elution of dichloromethane/methanol (0-5%, 500 ml). The fractions containing the product were combined and evaporated under reduced pressure to give a solid, (1.94 g), m.p. 130°-132°. Recrystallization from ethyl acetate gave the title compound, (1.7 g), m.p. 132°-133°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05049567 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-d6b2990135504790a9e44904127027a7 |
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| Source note | uspto-grants-1991_09 |
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