HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732249Generated: November 4, 2026
Sulfuric Acid → 1H-Isoindol-3-amine, 5,6-diethoxy-4-fluoro-, sulfate (1:1)
https://huagongshe.com/reaction/732249
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4,5-Diethoxy-3-fluorophthalonitrile | HCID 22929841 | — |
| Catalyst | HCID 178502593 | HCID 178502593 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 1H-Isoindol-3-amine, 5,6-diethoxy-4-fluoro-, sulfate (1:1) | HCID 11588054 | 72% |
Reaction Steps
A mixture of 4,5-diethoxy-3-fluorophthalonitrile (2.34 g, 10 mol) prepared in Preparation Example 1, sulfuric acid (0.56 mL, 10 mol), 20% palladium hydroxide-carbon (0.59 g, 50% hydrate) (20% palladium-carbon powder, palladium hydroxide type (hydrate), N.E. Chemical Corporation) and 1,2-dimethoxyethane (23 mL) was stirred at −23° C. under hydrogen atmosphere (atmospheric pressure) for 29 hours. After insoluble matter in the reaction mixture was filtered off, the residue was washed with methanol (23 mL), and the combined filtrate was divided into five equal portions. To one of them, triethylamine (0.14 mL, 1 mol) was added, and the mixture was stirred at 60° C. for three hours and concentrated at 40° C. under reduced pressure. Methanol (2.3 mL) and 1,2-dimethoxyethane (6.9 mL) were added to the residue, then sulfuric acid (0.11 mL, 2 mol) was added on ice, and the mixture was stirred. Precipitated crystals were filtered, washed with a 5% methanol-1,2-dimethoxyethane solution, and dried at room temperature under reduced pressure to give 0.45 g of the title compound (yield: 72%) as grayish white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07585982B2 |
|---|
| Source dataset | uspto-grants-2009_09 |
|---|
| ORD ID | ord-71d5a13e2cff468781edfaff52249ccd |
|---|
| Source note | uspto-grants-2009_09 |
|---|