HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876821Generated: October 29, 2026
Stannous chloride dihydrate → HCID 25014604, compound
https://huagongshe.com/reaction/1876821
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | HCID 66882276 | HCID 66882276 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 25014604 | HCID 25014604 | 139.9% |
Reaction Steps
[4-(Benzyloxy)-5-methoxy-2-nitrophenyl][4-(2-pyridyl)piperazino]methanone (7b) (500 mg, 1.11 mmol) was dissolved in methanol (10 mL), SnCl2.2H2O (753 mg, 3.3 mmol) was added and refluxed until the TLC indicated the completion of the reaction. The methanol was evaporated by vacuum and the aqueous layer was then adjusted to pH 8 with 10% NaHCO3 solution and extracted with ethyl acetate (2×30 mL). The combined organic phase was dried over Na2SO4 and evaporated under vacuum to afford the crude (450 mg, 95% yield), This was further purified by column chromatography using ethyl acetate:hexane (6:4) as a solvent system to obtain the pure product 8b (650 mg, in 94% yield). 1H NMR (CDCl3) δ 3.15-3.30 (m, 4H), 3.70-3.80 (m, 4H), 3.95 (s, 3H), 5.20 (s, 2H), 6.20 (s, br,) 7.00-7.50 (m, 5H), 7.70 (s, 1H), 8.25-8.35 (d, J=9.05, 2H); FABMS: 418 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08309726B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-781e23e2d1f04c38a9d3144adc407d58 |
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| Source note | uspto-grants-2012_11 |
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