Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 6-(Benzyloxy)-4-chloro-3-nitroquinoline | HCID 67050992 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 68900066 | HCID 68900066 | — |
Reaction Steps
Methylamine (available as a 40% solution in water, 24 mL, 0.28 mol) was added to a solution of 6-benzyloxy-4-chloro-3-nitroquinoline (15.0 g, 48.5 mmol), prepared as described in Parts A-D of Example 2, in distilled water (300 mL), and the reaction was stirred at 100° C. for 1.5 hours. The reaction was allowed to cool to ambient temperature and stirred for four hours. A precipitate formed, which was isolated by filtration and washed with distilled water (3×60 mL). The solid was combined with material from another run and recrystallized from 2-propanol. The crystals were isolated by filtration, washed twice with cold hexanes, and dried for three days under high vacuum to provide 24.10 g of (6-benzyloxy-3-nitroquinolin-4-yl)methylamine as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365567B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-1943548ed38f4a279af3ec03567956d0 |
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| Source note | uspto-grants-2016_06 |
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