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 Compound 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) δ 7.27 (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 | US07414071B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-05a0b573d9f1400cbadd1c1a8872e74a |
| Source note | uspto-grants-2008_08 |