Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Reactant | 5-Nitroindole-2-carboxylic acid | HCID 351291 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Solvent | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| Product | HCID 68023578 | HCID 68023578 | — |
Reaction Steps
Thionyl chloride (8 ml, 110 mmol, 5 eq.) was added to a suspension of the compound of formula (III) (4.53 g, 22 mmol, 1 eq.) in dry dioxane (50 ml). The final suspension was refluxed in dry atmosphere (CaCl2 valve) for 2 h, and the reaction turned to a light brown solution while proceeding. The reaction was cooled to 25° C. and organic volatiles were removed under reduced pressure, then dry toluene (25 ml) was added and removed under vacuum, this operation was repeated twice. The brown residue (22 mmol, 1 eq.) was added portion wise to a cooled solution at 0° C. of NaHCO3 (3.7 g, 43.95 mmol, 2 eq.) and 2,2-dimethoxy-ethylamine (2.39 ml, 21.97 mmol, 1 eq.) in dioxane/water 4:1 (100 ml), the suspension was stirred for 2 hours at rt. Organic volatiles were removed under reduced pressure and the yellow precipitate was filtered and dried to give 5-nitro-1H-indole-2-carboxylic acid (2,2-dimethoxy-ethyl)-amide (IV). Yield=5.80 g (90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08513241B2 |
|---|
| Source dataset | uspto-grants-2013_08 |
|---|
| ORD ID | ord-bbdd51e8671c429ab33699d0d610abab |
|---|
| Source note | uspto-grants-2013_08 |
|---|