HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431357Generated: November 3, 2026
Stannous chloride dihydrate → 5-Bromo-2-morpholinopyridin-3-amine
https://huagongshe.com/reaction/1431357
Participants
| Role | Name | HCID | Charge |
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| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | 4-(5-Bromo-3-nitropyridin-2-yl)morpholine | HCID 3145504 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Bromo-2-morpholinopyridin-3-amine | HCID 46737873 | — |
Reaction Steps
To a stirred mixture of 4-(5-bromo-3-nitropyridin-2-yl)morpholine (1.02 g, 3.54 mmol) in EtOAc (30 mL) was added tin(II) chloride dihydrate (4.01 g, 17.77 mmol) in portions. Upon complete addition of the reducing agent, the mixture was carefully heated to 90° C. After 2 h, the reaction was cooled to rt and diluted with ethyl acetate, then washed with 1M NaOH, water, and brine. After drying over anhydrous sodium sulfate and filtration, the organic solvent was removed under reduced pressure. The residue was identified as 5-bromo-2-morpholinopyridin-3-amine. 1H NMR (400 MHz, DMSO-d6) δ ppm 7.59 (1H, d, J=2.0 Hz), 7.12 (1H, d, J=2.0 Hz), 5.19 (2H, s), 3.80 (4H, m), 3.02 (4H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940724B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-cfd583af70354925b83791187d9f71fb |
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| Source note | uspto-grants-2015_01 |
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