HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762807Generated: November 2, 2026
Naphthazarin diacetate → HCID 20039729, compound
https://huagongshe.com/reaction/1762807
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Naphthazarin diacetate | HCID 273064 | — |
| Reactant | 2-Formyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid | HCID 12324171 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 20039729 | HCID 20039729 | 41.4% |
Reaction Steps
5,8-bis(acetyloxy)-1,4-napthalenedione (4.28 g) and 2-formyl-1,2,3,4-tetrahydro-3-isoquinoline carboxylic acid (1.60 g) in acetic anhydride (65 ml) were heated at 100° C. (20 minutes). The reaction mixture was cooled at about 20° C. (1 h), and the solid was collected by filtration, washed with ether (3×30 ml) and dried in vacuo. The crude product was dissolved in dichloromethane and the solution was loaded onto a column of silica gel (175 g) packed in dichloromethane. The column was eluted with 5% (v/v) ethyl acetate in dichloromethane and fractions containing the major component were evaporated to dryness, and further dried in vacuo at 55° C. to give the title compound as a yellow-green solid (1.34 g), m.p. 228°-232° C. (dec), λmax (in CH2Cl2) 242 nm (ε40,700), 377 nm (ε6,400).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04835158 |
|---|
| Source dataset | uspto-grants-1989_05 |
|---|
| ORD ID | ord-01cfc379a9434596b41ddf612a4d7893 |
|---|
| Source note | uspto-grants-1989_05 |
|---|