HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 2974347, compound → HCID 57438148, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 2974347 | HCID 2974347 | — |
| Reactant | HCID 22272508 | HCID 22272508 | — |
| Catalyst | Nickel | HCID 935 | — |
| Product | HCID 57438148 | HCID 57438148 | 90% |
Reaction Steps
N-Ethyl-5-(4-methyl-1-piperazinyl)-2-nitroaniline was reduced with Raney-Ni as described previously for the synthesis of tert-butyl 4-[4-amino-3-(ethylamino)phenyl]-1-piperazinecarboxylate to give N-2-ethyl-4-(4-methyl-1-piperazinyl)-1,2-benzenediamine (yield>90%) as a red oil. The product is very sensitive to oxidation and was therefore used immediately in the next reaction step. HPLC purity>90%; MS (posEI) m/z=234 (M+);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07173035B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-9bfaffa4d2394bf89e33615ea1c662c8 |
| Source note | uspto-grants-2007_02 |