HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzyl alcohol → 2-Chlorobenzyl cis-2,6-dimethylpiperazine-1-carboxylate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzyl alcohol | HCID 28810 | — |
| Reactant | rel-1,1-Dimethylethyl (3R,5S)-4-(chlorocarbonyl)-3,5-dimethyl-1-piperazinecarboxylate | HCID 86585999 | — |
| Product | 2-Chlorobenzyl cis-2,6-dimethylpiperazine-1-carboxylate hydrochloride | HCID 69141343 | — |
Reaction Steps
2-Chlorobenzyl cis-2,6-dimethylpiperazine-1-carboxylate hydrochloride was prepared from cis 1-chlorocarbonyl-2,6-dimethyl-4-tert-butoxycarbonylpiperazine and 2-chloro-benzyl alcohol according to the methods described for Examples 52 and 54 to give the product as a white solid (0.0901 g, 14% overall); νmax (nujol)/cm−1 3375, 2689, 2577, 1699, 1592, 1380, 1328, and 1300; δH (400 MHz, DMSO-d6) 9.62 (2 H, br), 7.50 (2 H, m), 7.40 (2 H, m), 5.19 (2 H, s), 4.33 (2 H, m), 3.18–3.06 (4 H, m), and 1.31 (6 H, d, J 7.2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07022707B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-c211103c826e42b493b5a51a803010d1 |
| Source note | uspto-grants-2006_04 |