HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773920Generated: November 3, 2026
Stannous chloride dihydrate → HCID 86704004, compound
https://huagongshe.com/reaction/1773920
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | HCID 86704005 | HCID 86704005 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86704004 | HCID 86704004 | — |
Reaction Steps
A mixture of 4-(1-methylpiperidin-4-yloxy)-8-(3-nitrophenyl)-2-phenyl-9,10-dihydro-4H-3,10a-diaza-benzo[f]azulene (example 242 B) (0.6 mmole), tin(II) chloride dihydrate (2.83 g) in ethanol (15 mL) is refluxed for 2 hours. The mixture is then cooled to room temperature and extracted twice with chloroform. Pooled organic extracts are dried over magnesium sulphate, filtered and the solvent is removed under reduced pressure. The residue is purified by preparative HPLC-MS (Waters AutoPurification HPLC/MS System, Sunfire Prep C18 5 μm OBD 30×150 mm column, eluents: water/0.1% formic acid (A) and acetonitrile/0.1% formic acid (B), focus gradient from 14% (B) to 24% (B) in 10 minutes) to afford 3-[4-(1-methylpiperidin-4-yloxy)-2-phenyl-9,10-dihydro-4H-3,10a-diaza-benzo[f]azulen-8-yl]-phenylamine melting at 120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09255101B2 |
|---|
| Source dataset | uspto-grants-2016_02 |
|---|
| ORD ID | ord-62121426afdd42809c89b2a897ea9f22 |
|---|
| Source note | uspto-grants-2016_02 |
|---|