HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 22477457, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 178427315 | HCID 178427315 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22477457 | HCID 22477457 | 43.4% |
Reaction Steps
To a suspension of N-hydroxy-1-methyl-3-[1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridin-2-yl]-1H-indole-5-carboxamidine [0.7 g, Reference Example 26] in toluene (30 mL) at ambient temperature under nitrogen was added acetic anhydride (0.467 g). The reaction mixture was heated at reflux for 4.5 hours then filtered. The filtrate was evaporated to give the title compound (0.32 g) as a dark red oil which was used immediately without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07943616B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-dec6b530fdb04a739b0fa9fa9b5f7c68 |
| Source note | uspto-grants-2011_05 |