HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711671Generated: October 25, 2026
4-Methoxybenzylamine → 4-Amino-2-oxo-1,2-dihydroquinoline-3-carbonitrile
https://huagongshe.com/reaction/711671
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methoxybenzylamine | HCID 75452 | — |
| Reactant | 4-Chloro-1,2-dihydro-2-oxoquinoline-3-carbonitrile | HCID 2777510 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Amino-2-oxo-1,2-dihydroquinoline-3-carbonitrile | HCID 5200312 | 25.1% |
Reaction Steps
4-chloro-2-oxo-1,2-dihydroquinoline-3-carbonitrile (example 72) (0.66 g, 3.23 mmol) was suspended in DMF (7 mL), and 4-methoxybenzylamine (0.94 mL, 7.26 mmol) was added. The reaction was heated at 100° C. for 1 hour and the DMF was removed under vacuum. The residue was dissolved in TFA (6 mL) and stirred at room temperature for 30 minutes and dichloromethane (10 mL) was added. The solid product that formed was collected, suspended in water and the solution stirred overnight. The solid was collected by filtration to give 4-amino-2-oxo-1,2-dihydroquinoline-3-carbonitrile (0.150 g, 25%) as a white solid. M.p.: >250° C. 1H NMR (400 MHz, DMSO-d6) δ 7.19 (m, 2H), 7.57 (m, 1H), 7.88 (bs, 2H), 8.12 (d, J=7.6 Hz, 1H), 11.23 (s, 1H). MS 186 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181276B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-35534af4bc214111bacea8dea69db3ac |
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| Source note | uspto-grants-2015_11 |
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