HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620232Generated: October 30, 2026
Isopropylamine → 2-(Isopropylamino)-6-methoxyquinoline-3-carbaldehyde
https://huagongshe.com/reaction/1620232
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | 2-Chloro-6-methoxyquinoline-3-carbaldehyde | HCID 689079 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Isopropylamino)-6-methoxyquinoline-3-carbaldehyde | HCID 86669820 | 99.2% |
Reaction Steps
To a stirred solution of 2-chloro-6-methoxyquinoline-3-carbaldehyde (1.50 g, 6.77 mmol) in THF (10 mL) in a 20 mL microwave vial equipped with a magnetic stirrer was added propan-2-amine (5.76 mL, 67.7 mmol) and the reaction mixture was stirred for 12.5 h at 160° C. and finally 45 min at 180° 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. The volatiles were then removed at 40° C. under vacuum and the residue was then neutralised with a saturated NaHCO3 aqueous solution before extraction with CH2Cl2 (100 mL). The organic layer was washed with brine (20 mL), dried over MgSO4, filtered, and concentrated under vacuum to give 2-(isopropylamino)-6-methoxyquinoline-3-carbaldehyde SLA 28186 as an orange solid (1.64 g, 99% 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-c1885b70b7e5438fa4ebd0560a1d6e71 |
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| Source note | uspto-grants-2014_07 |
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