HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859611Generated: October 26, 2026
Gamma-Butyrolactone → 8-(4-Fluoro-phenyl)-4-{3-[5-(3-hydroxy-propyl)-[1,2,4]oxadiazol-3-yl]-phenyl}-1,3-dihydro-benzo[b][1,4]diazepin-2-one
https://huagongshe.com/reaction/859611
Participants
| Role | Name | HCID | Charge |
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| Reactant | Gamma-Butyrolactone | HCID 7302 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178513288 | HCID 178513288 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 8-(4-Fluoro-phenyl)-4-{3-[5-(3-hydroxy-propyl)-[1,2,4]oxadiazol-3-yl]-phenyl}-1,3-dihydro-benzo[b][1,4]diazepin-2-one | HCID 22224599 | 65.7% |
Reaction Steps
To a stirred suspension of 3-[7-(4-fluoro-phenyl)-4-oxo-4,5-dihydro-3H-benzo[b][1,4]diazepin-2-yl]-N-hydroxy-benzamidine (Example 167) (78 mg, 0.2 mmol) in EtOH (3 mL) was added at 23° C. sodium hydride (55% dispersion in oil, 32 mg, 0.8 mmol) and the mixture was stirred at 23° C. for 5 min. Butyrolactone (103 mg, 1.2 mmol) was added and the mixture was heated to 70° C. for 3 h. The reaction mixture was cooled to 23° C. and partitioned between ethyl acetate and H2O. The organic layer was dried over Na2SO4, evaporated in vacuum, and the residue was crystallized from dichloromethane to give the title compound as light yellow solid (60 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07151098B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-d2e4c00965cd4ee9b88a364cdc2a4560 |
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| Source note | uspto-grants-2006_12 |
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