HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Methoxy-2-(trifluoromethyl)pyrazolo[1,5-a]pyridine-4-carbaldehyde → 4-(1-Hydroxypropyl)-7-methoxy-2-trifluoromethyl-pyrazolo[1,5-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Methoxy-2-(trifluoromethyl)pyrazolo[1,5-a]pyridine-4-carbaldehyde | HCID 59389351 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Product | 4-(1-Hydroxypropyl)-7-methoxy-2-trifluoromethyl-pyrazolo[1,5-a]pyridine | HCID 59389385 | — |
Reaction Steps
The compound of Example 115 was reacted with ethyl magnesium bromide as in Example 134 to afford the title compound as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07763617B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-9db7c104fc4d4d16b282a1630c9892fb |
| Source note | uspto-grants-2010_07 |