Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thioacetamide | HCID 2723949 | — |
| Reactant | HCID 86602841 | HCID 86602841 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11710687 | HCID 11710687 | 80% |
Reaction Steps
(R)-4-(2-Bromo-acetyl)-1-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one (0.040 g, 0.098 mmol) was dissolved in tetrahydrofuran (1 ml) and thioacetamide (0.007 g, 0.098 mmol) was added and the mixture was stirred at 40° C. for 24 hours. The tetrahydrofuran was evaporated and the residue was purified by column chromatography on silica gel using at first a 1:1-mixture then a 4:1-mixture of ethyl acetate and hexane as the eluent to yield the title compound as a light yellow solid (0.030 g, 80% of theory). MS (m/e)=383.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07456210B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-7bc6f52a2eff479b914db18a4ad4ba0b |
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| Source note | uspto-grants-2008_11 |
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