HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalic Anhydride → HCID 58054415, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | 4-Methoxy-1H-indazol-3-amine | HCID 18526053 | — |
| Reactant | 1,1-dimethylethyl 3-{bis[(5-chloro-2-thienyl)sulfonyl]amino}-4-(methyloxy)-1H-indazole-1-carboxylate | HCID 58054456 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 58054415 | HCID 58054415 | 81% |
Reaction Conditions
| Temperature | 110 °C |
|---|
Reaction Steps
4-(Methyloxy)-1H-indazol-3-amine (for a preparation see Intermediate 1) (500 mg, 3 mmol) and phthalic anhydride (680 mg, 4.6 mmol) (available from Aldrich) were dissolved in 1,4-dioxane (5 mL) at room temperature. The reaction mixture was stirred at 110° C. overnight, and then it was cooled and concentrated under reduced pressure. The residue was triturated and sonicated with 50 mL of ether. The solid was collected by filtration and dried in a vacuum oven to obtain a brown solid (711 mg, 81%). LCMS (System B) RT=2.82 min, ES+ve m/z 294 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08357716B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-99ee58fa12da4e3ea9ffabf1f8dd8127 |
| Source note | uspto-grants-2013_01 |