Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Reactant | HCID 135829355 | HCID 135829355 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 135829358 | HCID 135829358 | 69.8% |
Reaction Steps
To a solution of (3RS)-3-acetoxy-5-cyclohexyl-2,3-dihydro-1H-1,4-benzodiazepin-2-one (2.00 g) in N,N-dimethylformamide (15 ml) was added potassium phthalimide (1.85 g) under stirring and heated at 60° C. To the mixture was added sodium iodide (12.64 g) and stirred for 3 hours at 100° C. The hot resultant mixture was poured into ice-water to give a crude product. The precipitated crude product was collected by filtration. Dryness under the reduced pressure at 40° C. gave (3RS)-5-cyclohexyl-2,3-dihydro-3-phthalimido-1H-1,4-benzodiazepin-2-one (1.80 g) as an yellow powder, which was used in a following reaction step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05763437 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-c232821b2f9549e981d754a71157e4b3 |
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| Source note | uspto-grants-1998_06 |
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