HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dihydroxybenzaldehyde → HCID 86637669, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dihydroxybenzaldehyde | HCID 7213 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 59139440 | HCID 59139440 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86637669 | HCID 86637669 | 666.5% |
Reaction Steps
(3-Acetylaminophenylsulfamoyl)acetic acid ethyl ester (280 mg, 0.93 mmol), 2,4-dihydroxybenzaldehyde (516 mg) and piperidine (10 mg) were added to 9 mL of ethanol, and the mixture was heated under reflux overnight. It was then purified by silica gel chromatography (methylene chloride:methanol=30:1) to yield the title compound (304 mg, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897792B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-60b665497c754f20aa0f36151bd9cdd2 |
| Source note | uspto-grants-2011_03 |