HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Benzyloxy)benzaldehyde → 4-(2-Benzyloxy-benzyl)-piperazine-1-carboxylic acid phenylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Benzyloxy)benzaldehyde | HCID 344784 | — |
| Reactant | N-phenylpiperazine-1-carboxamide | HCID 7015289 | — |
| Product | 4-(2-Benzyloxy-benzyl)-piperazine-1-carboxylic acid phenylamide | HCID 57880873 | — |
Reaction Steps
The title compound was prepared from piperazine-1-carboxylic acid phenylamide and 2-benzyloxybenzaldehyde. 1H NMR (400 MHz, CDCl3): 7.49-7.20 (m, 11H), 7.05-6.92 (m, 3H), 6.41 (s, 1H), 5.08 (s, 2H), 3.65 (s, 2H), 3.51-3.45 (m, 4H), 2.55-2.49 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09169224B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-5ab48e4da02a4026a7bcdb6d3ef3e306 |
| Source note | uspto-grants-2015_10 |