HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518622Generated: October 30, 2026
Stannous Chloride → HCID 178461584, compound
https://huagongshe.com/reaction/518622
Participants
| Role | Name | HCID | Charge |
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| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | HCID 178461585 | HCID 178461585 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178461584 | HCID 178461584 | 100.2% |
Reaction Steps
To a suspension of (R)-tert-butyl 3-methyl-4-(cis-4-(5-nitro-2-(2-(piperidin-1-yl)ethoxy)pyridin-4-ylamino)cyclohexanecarbonyl)piperazine-1-carboxylate (0.2 g, 0.348 mmol) in MeOH (3.48 mL) was added tin(II) chloride (0.264 g, 1.392 mmol). The resulting suspension was stirred at 80° C. for 2 hours. The mixture was cooled to RT, diluted with EtOAc and washed with 1N aqueous NaOH. The organic layer was collected, dried over sodium sulfate and concentrated to afford (R)-tert-butyl 4-(cis-4-(5-amino-2-(2-(piperidin-1-yl)ethoxy)pyridin-4-ylamino)cyclohexanecarbonyl)-3-methylpiperazine-1-carboxylate as a tan solid (190 mg, 100%). MS m/z=545.4 [M+H]. Calc'd for C29H48N6O4: 544.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115127B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-f19a570faa56402aaa68eb0dd41ca11e |
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| Source note | uspto-grants-2015_08 |
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