HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620196Generated: October 25, 2026
Methylamine → 6-Methoxy-2-(methylamino)quinoline-3-carbaldehyde
https://huagongshe.com/reaction/1620196
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 2-Chloro-6-methoxyquinoline-3-carbaldehyde | HCID 689079 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-Methoxy-2-(methylamino)quinoline-3-carbaldehyde | HCID 86669816 | 98.4% |
Reaction Steps
To a stirred solution of 2-chloro-6-methoxyquinoline-3-carbaldehyde (1.50 g, 6.77 mmol) in 1,4-dioxan (10 mL) in a 20 mL microwave vial equipped with a magnetic stirrer was added methylamine (40 wt % solution in water, 2.10 mL, 24.3 mmol) and the reaction mixture was stirred for 6 h at 160° C. under microwave irradiation. After cooling to RT, the volatiles were removed at 40° C. under vacuum and the resulting yellow oil was taken up in a mixture of THF:1 N aq. HCl=1:1 (50 mL) and stirred for 1 h at RT. THF was removed at 40° C. under vacuum and the residue was then neutralised with a saturated NaHCO3 aqueous solution before to be extracted with CH2Cl2 (100 mL). The organic phase was washed with brine (20 mL), dried over MgSO4, filtered, and concentrated under vacuum, to give 6-methoxy-2-(methylamino)quinoline-3-carbaldehyde SLA 28150 as an orange oil (1.44 g, 98% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772316B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-0f3fb6519888473c9e09461f52d15de5 |
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| Source note | uspto-grants-2014_07 |
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