HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl bromoacetate → (Butyl-[4-(4-oxo-piperidin-1-yl)-benzenesulfonyl]-amino)-acetic acid benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl bromoacetate | HCID 62576 | — |
| Reactant | N-butyl-4-(4-oxo-piperidin-1-yl)-benzenesulfonamide | HCID 12051795 | — |
| Product | (Butyl-[4-(4-oxo-piperidin-1-yl)-benzenesulfonyl]-amino)-acetic acid benzyl ester | HCID 69899200 | — |
Reaction Steps
The title compound was prepared from N-butyl-4-(4-oxo-piperidin-1-yl)-benzenesulfonamide ( ) and benzyl bromoacetate according to the procedure of Intermediate 2 as a gum; 1H NMR (CDCl3) δ 0.85 (t, J=7.23 Hz, 3H), 1.19-1.32 (m, 2H), 1.43-1.53 (m, 2H), 2.56 (t, J=6.12 Hz, 4H), 3.19 (t, J=7.47 Hz, 2H), 3.72 (t, J=6.06 Hz, 4H), 4.09 (s, 2H), 5.10 (s, 2H), 6.84-6.89 (m, 2H), 7.29-7.40 (m, 5H), 7.69-7.74 (m, 2H); MS (ES) m/z 45.94 (MH+); HRMS for C25H30N2O6S: 459.1945 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06444685B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-435e1e9afae6488f81b2b996ff453199 |
| Source note | uspto-grants-2002_09 |