HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273197Generated: October 31, 2026
Ammonium Chloride → 1-(6-methoxy-3,4-dihydro-2H-1-oxa-9-aza-phenanthren-3-yl)-1H-pyrazol-4-ylamine
https://huagongshe.com/reaction/2273197
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 6-methoxy-3-(4-nitro-pyrazol-1-yl)-3,4-dihydro-2H-1-oxa-9-aza-phenanthrene | HCID 67248260 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(6-methoxy-3,4-dihydro-2H-1-oxa-9-aza-phenanthren-3-yl)-1H-pyrazol-4-ylamine | HCID 68315046 | 22% |
Reaction Steps
Ammonium chloride (4.0 g, 73.54 mmol, 6.0 eq) is added at room temperature to a stirred suspension of 6-methoxy-3-(4-nitro-pyrazol-1-yl)-3,4-dihydro-2H-1-oxa-9-aza-phenanthrene (4.0 g, 12.26 mmol, 1.0 eq) and iron powder (8.22 g, 147.10 mmol, 12.0 eq) in ethanol (600 mL). The resulting mixture is heated under reflux for 2 hours, then filtered through decalite, solvent is removed and the crude is extracted with ethyl acetate (3×200 mL) and water (200 mL). The combined organic layers are dried over sodium sulfate, filtered and concentrated to give a residue that is purified by column chromatography (silica gel, eluent: petroleum ether:ethyl acetate:methanol, 1:1:0 to 0:25:1, v/v/v) to afford 1-(6-methoxy-3,4-dihydro-2H-1-oxa-9-aza-phenanthren-3-yl)-1H-pyrazol-4-ylamine as a white solid (800 mg, 22% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120822B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-68d702bd94294249b1df2d1e168c28be |
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| Source note | uspto-grants-2015_09 |
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