HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657060Generated: October 31, 2026
Sodium Sulfate → 6-{[({(3S)-1-[2-(7-fluoro-2-oxo-1(2H)-quinolinyl)ethyl]-3-pyrrolidinyl}methyl)amino]methyl}-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one
https://huagongshe.com/reaction/657060
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 3-Oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine-6-carbaldehyde | HCID 21873737 | — |
| Reactant | 1-{2-[(3S)-3-(Aminomethyl)-1-pyrrolidinyl]ethyl}-7-fluoro-2(1H)-quinolinone | HCID 68817941 | — |
| Product | 6-{[({(3S)-1-[2-(7-fluoro-2-oxo-1(2H)-quinolinyl)ethyl]-3-pyrrolidinyl}methyl)amino]methyl}-2H-pyrido[3,2-b][1,4]oxazin-3(4H)-one | HCID 57927990 | 51% |
Reaction Steps
To a solution of 1-{2-[(3S)-3-(aminomethyl)-1-pyrrolidinyl]ethyl}-7-fluoro-2(1H)-quinolinone (87 mg, 0.30 mmol) and 3-oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine-6-carboxaldehyde (for a synthesis see WO2003087098, Example 31(e)) (54 mg, 0.302 mmol) was added Na2SO4 (355 mg, 2.50 mmol) and the reaction was stirred at ambient temperature for 18 h. The intermediate imine was treated with sodium triacetoxyborohydride (160 mg, 0.75 mmol) and stirred for an additional 16 h). The solvents were removed under reduced pressure; the residue was partitioned between dichloromethane and aqueous sodium bicarbonate, and the organic layer was dried (Na2SO4). Purification by column chromatography on silica gel, (1% to 20% methanol:dichloromethane gradient) yielded the title compound as an amorphous off-white solid (69 mg, 51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071592B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-e9bf17c4f9e54d65a4b30d8e2704f846 |
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| Source note | uspto-grants-2011_12 |
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