HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21864857, compound → HCID 66894206, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21864857 | HCID 21864857 | — |
| Reactant | HCID 66891841 | HCID 66891841 | — |
| Product | HCID 66894206 | HCID 66894206 | — |
Reaction Steps
Reduction of the nitro group in N,N-diethyl-2-[4-(5-nitro-1-benzofuran-7-yl)piperazin-1-yl]acetamide (0.3 g, 0.83 mmol; Intermediate 22) was performed according to the procedure of Intermediate 10. Yield: 0.19 g (70%). This material was used in the next step without further purification. MS (ESI+) m/z 331.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820675B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-211ed25683a3458b9f750fa4f28a6ced |
| Source note | uspto-grants-2010_10 |