HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-(Benzyloxy)phenyl)hydrazine monohydrochloride → 1-(4-Benzyloxyphenyl)-8-methoxy-3-methyl-4,5-dihydro-1H-benzo[g]indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-(Benzyloxy)phenyl)hydrazine monohydrochloride | HCID 3016725 | — |
| Reactant | 2-Acetyl-7-methoxy-3,4-dihydro-2H-naphthalen-1-one | HCID 19095398 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(4-Benzyloxyphenyl)-8-methoxy-3-methyl-4,5-dihydro-1H-benzo[g]indazole | HCID 58948767 | 32.1% |
Reaction Steps
2-Acetyl-7-methoxy-3,4-dihydro-2H-naphthalen-1-one (72.5 mg, 0.33 mmol) and 4-benzyloxyphenylhydrazine hydrochloride (90 mg, 0.36 mmol) were heated in ethanol at 70° C. for 2.5 days. The reaction was diluted with water and extracted with ethyl acetate. The organic extracts were washed with 1 N HCl, saturated sodium bicarbonate solution, and brine, dried over MgSO4, and concentrated. SiO2 chromatography with 5-20% ethyl acetate/hexanes gave 42 mg of the desired product. LC-MS (C26H24N2O2 calculated 396) m/z 397 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897634B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-53c9d3b1802d425ca29fb5e81984c91c |
| Source note | uspto-grants-2011_03 |