HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Hydroxy-2-pentanone → HCID 21449343, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Hydroxy-2-pentanone | HCID 14066 | — |
| Reactant | HCID 86734555 | HCID 86734555 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21449343 | HCID 21449343 | — |
Reaction Steps
A solution of acetaldehyde N1 -(7-chloroquinazolin-4-yl)p-methoxyphenylhydrazone hydrochloride (3.2g.) and 5-hydroxy-pentane-2-one (1.1g.) in ethanol (60ml.) was refluxed for 18 hours. The mixture was cooled and filtered and the filtrate evaporated in vacuo. The residue was chromatographed on silica gel (100g.) using, as eluant, petroleum ether (b.p. 40° -60° C.) containing an increasing proportion of ether (polarity increased by incremental addition of 10% v/v ether) to give 1-(7-chloroquinazolin-4-yl)-3-(2-hydroxyethyl)-5-methoxy-2-methylindole, m.p. 148°-150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04012513 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-4cd57e6b87b44399bb594949dd5a8a41 |
| Source note | uspto-grants-1977_03 |