HuagongsheHuagongshe Chemistry Print Report · For research reference only
Rolziracetam → 5-[4-(3-Chloro-phenyl)-3-oxo-butyl]-pyrrolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Rolziracetam | HCID 71893 | — |
| Reactant | HCID 178478996 | HCID 178478996 | — |
| Product | 5-[4-(3-Chloro-phenyl)-3-oxo-butyl]-pyrrolidin-2-one | HCID 12970090 | 51.5% |
Reaction Steps
Analogous to the procedure described for Example 1A, Step A, tetrahydro-pyrrolizine-3,5-dione (2 g, 14 mmol) was reacted with 3-chlorobenzylmagnesium chloride (0.25M in Et2O, 62 mL, 15.5 mmol) over 2 h. Purification by medium pressure chromatography eluting with a solvent gradient (2:1 hexanes:EtOAc to EtOAc to 5% MeOH in CH2Cl2) provided 5-[4-(3-chloro-phenyl)-3-oxo-butyl]-pyrrolidin-2-one (1.9142 g). 1H NMR (CDCl3) δ7.27 (m, 2H), 7.19 (m, 1H), 7.08 (m, 1H), 6.27 (br, 1H), 3.68 (s, 2H), 3.60 (m, 1H), 2.52 (t, 2H), 2.29 (m, 2H), 2.21 (m, 1H), 1.88–1.60 (m, 3H); MS 266.2 (M+1), 264.2 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07192979B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-9195e8192a21462a8157fdedfc9fcf16 |
| Source note | uspto-grants-2007_03 |