HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromobenzaldehyde → 4-(3-Bromo-benzyl)-piperazine-1-carboxylic acid phenylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromobenzaldehyde | HCID 76583 | — |
| Reactant | N-phenylpiperazine-1-carboxamide | HCID 7015289 | — |
| Product | 4-(3-Bromo-benzyl)-piperazine-1-carboxylic acid phenylamide | HCID 17185125 | — |
Reaction Steps
The title compound was prepared from piperazine-1-carboxylic acid phenylamide and 3-bromobenzaldehyde. 1H NMR (400 MHz, CDCl3): 7.50 (br s, 1H), 7.43-7.17 (m, 7H), 7.05-7.00 (m, 1H), 6.47 (br s, 1H), 3.52-3.45 (m, 6H), 2.48-2.42 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08530476B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-be19c54a6a7b4363ad6e79a44808b534 |
| Source note | uspto-grants-2013_09 |