Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | 5-Hydroxy-6-methoxy-2,3-dihydro-1H-inden-1-one | HCID 14763395 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Product | HCID 15721804 | HCID 15721804 | — |
Reaction Steps
1,4-Dihydroindeno[1,2-c]pyrazoles of general formula (13), wherein X3, R4, R5, and R6 are as defined in formula (I), can be prepared as described in Scheme 3. 5,6-Dimethoxy-1-indanone, purchased from Aldrich Chemical Co., can be treated with sodium cyanide to provide 5-hydroxy-6-methoxy-1-indanone. 5-Hydroxy-6-methoxy-1-indanone can be treated with nitric acid and sodium nitrite to provide 5-hydroxy-6-methoxy-4-nitro-1-indanone. 5-Hydroxy-6-methoxy-4-nitro-1-indanone can be treated with iodomethane and then methodology described in Scheme 2 to provide compounds of general formula (12). Compounds of general formula (12) can be treated with a reducing agent, including iron metal in the presence of acetic acid, to provide amines of general formula (13).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07320986B2 |
|---|
| Source dataset | uspto-grants-2008_01 |
|---|
| ORD ID | ord-db3b4896eec840e4b794d2c6e909fa5a |
|---|
| Source note | uspto-grants-2008_01 |
|---|