HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2,3-dihydro-5-methoxy-1H-indole-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | (RS)-5-methoxy-2,3-dihydro-1H-indole-2-carboxylic acid methyl ester | HCID 54121458 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,3-dihydro-5-methoxy-1H-indole-2-carboxamide | HCID 21914088 | — |
Reaction Steps
2,3-dihydro-5-methoxy-1H-indole-2-carboxylic acid methyl ester (0.084 mole) and 2M NH3 in methanol (500 ml) were combined and stirred at room temperature under argon over the weekend. The solution was concentrated to 100 ml, cooled in an ice bath, and filtered. The solid was rinsed with a small amount of cold methanol and dried. The residue was triturated in methanol/ACN and filtered, yielding 4.56 g of 2,3-dihydro-5-methoxy-1H-indole-2-carboxamide (intermediate 21, mp. 228–229° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07125891B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-9543eba8d91f4bc097ad74bacf56dded |
| Source note | uspto-grants-2006_10 |