HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Methylsulfonyl)benzyl Bromide → HCID 58797590, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Methylsulfonyl)benzyl Bromide | HCID 2733581 | — |
| Reactant | Tert-butyl 4-(2H-tetrazol-5-YL)piperidine-1-carboxylate | HCID 18187701 | — |
| Reactant | HCID 58797593 | HCID 58797593 | — |
| Product | HCID 58797590 | HCID 58797590 | — |
Reaction Steps
This was prepared from 4-methanesulphonylbenzyl bromide and tert-butyl 4-(2H-tetrazol-5-yl)piperidine-1-carboxylate using a similar method to that used to prepare 4-[2-(4-chloro-benzyl)-2H-tetrazol-5-yl]-piperidine (Method G, Steps 4 and 5); NMR (CDCl3): 1.8 (m, 2H), 2.05 (m, 2H), 2.8 (m, 2H), 3.05 (s, 3H), 3.1 (m, 1H), 3.2 (m, 2H), 5.89 (s, 2H), 7.55 (d, 2H), 7.95 (d, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07294636B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-87564830a2fd431892235545d6e9fa6f |
| Source note | uspto-grants-2007_11 |