HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876820Generated: November 2, 2026
Stannous chloride dihydrate → HCID 24206030, compound
https://huagongshe.com/reaction/1876820
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | HCID 66882955 | HCID 66882955 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 24206030 | HCID 24206030 | 91.3% |
Reaction Steps
[4-(Benzyloxy)-5-methoxy-2-nitrophenyl][4-(2-methoxyphenyl)piperazino]methanone (7a) (500 mg, 1.04 mmol) was dissolved in methanol (10 mL), SnCl2.2H2O (706 mg, 3.14 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. This was further purified by column chromatography using ethyl acetate:hexane (6:4) as a solvent system to obtain the pure product (8a) (425 mg, 91% yield). 1H NMR (CDCl3) δ 3.20-3.30 (m, 4H), 3.45-3.55 (m, 4H), 3.85 (s, 3H), 3.98 (s, 3H), 5.20 (s, 2H), 6.19 (s, broad NH2) 6.80-7.00 (m, 5H), 7.30-7.50 (m, 5H), 7.70 (s, 1H); FABMS: 447 (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-1ca993422ed949659306c322c86d9a6a |
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| Source note | uspto-grants-2012_11 |
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